Altrazeal® is a patented powder dressing specially engineered to cover and protect the wound and to provide an ideal moist wound healing environment that supports cellular function and tissue repair. Its non-resorbable, sterile granules aggregate when hydrated with saline to form a moist, flexible, oxygen permeable film that fits and seals the wound.
The skin-like barrier serves many functions that promote healthy granulation tissue growth:
1. seals and protects the entire wound surface
2. allows oxygen transportation
3. manages exudate through vapor transpiration
4. prevents penetration of exogenous bacteria
Altrazeal® enables extended wear time, allowing the wound to heal without disturbing the wound bed with frequent dressing changes.
OneTouch Select Plus Flex® meter uses BLUETOOTH®SMARTâ? wireless technology to pair and send glucose results to the OneTouch Reveal® mobile app* which makes reviewing and tracking blood sugar information easy when you're on the go
*The low and high range limits you set apply to all glucose test results. This includes tests taken before or after mealtimes, medication and around any other activities that may affect blood glucose. Patients are advised to talk to their healthcare professional about the low and high limits that are right for them.
â? The Bluetooth® word mark and logos are registered trademarks owned by Bluetooth SIG, Inc. and any use of such marks by LifeScan Scotland is under licence. Other trademarks and trade names are those of their respective owners.
* Please contact your healthcare professional for the availability in your country of residence. Other trademarks and trade names are those of their respective owners.
OneTouch Select Plus Flex® meter (CR2032 lithium coin cell battery included)
10 OneTouch Select Plus® test strips
OneTouch® Delica® lancing device
10 OneTouch® Delica® sterile lancets
Owner's Booklet
Get Started Guide
Carry case
One Touch Ultra Strip is a part of One Touch device. When used with One Touch meters, these strips measure the concentration of blood glucose by self-testing for both professional and home use.
Salient Features:
Automatically draws blood into the test strips in a painless manner
Fast, painless testing
For quick and accurate results
Pack Size: 50 strips & 10 strips
Warranty: 6 months
Directions For Use:
OneTouch Ultra Strips are used with the OneTouch Meter for quantitatively measuring glucose in fresh capillary whole blood
These Strips and meter are intended for self testing outside the body (in vitro diagnostic use) by people with diabetes at home and health care professionals in the clinical setting, as an aid to monitor the effectiveness of diabetes control
OneTouch Ultra Strips and meter are for use on the finger, palm, and forearm
Safety Information:
Each strip intended for single one time use
Keep out of the reach and sight of the children
Dispose the used strips properly
Store in a cool and dry place
The OneTouch® Selectâ?¢ Plus Blood Glucose Monitoring System is intended to be used for the quantitative measurement of glucose (sugar) in fresh capillary whole blood samples drawn from the fingertip.
The system is intended to be used by a single patient and should not be shared. The OneTouch® Selectâ?¢ Plus Blood Glucose Monitoring System is intended for self-testing outside the body (in vitro diagnostic use) by people with diabetes at home and with their healthcare professionals in a clinical setting as an aid to monitor the effectiveness of diabetes control.
The OneTouch® Selectâ?¢ Plus Blood Glucose Monitoring System is not to be used for the diagnosis of or screening of diabetes or for neonatal use. The system is intended to be used by a single patient and should not be shared.
Test Principle
Glucose in the blood sample mixes with the enzyme Glucose Oxidase (see page 130) in the test strip and a small electric current is produced.
The strength of this current changes with the amount of glucose in the blood sample. Your meter measures the current, calculates your blood glucose level, displays the blood glucose result, and stores it in its memory. Use only OneTouch® Selectâ?¢ Plus Control Solutions and Test Strips with the OneTouch® Selectâ?¢ Plus Meter.
OneTouch select plus 50 strips. Select plus siple glucometer strips. New OneTouch select plus simple. So simple, it's advanced
Uses
It helps to monitor the blood glucose level with comfort at home and helps in keeping diabetes and related issues in check.
Salient Features:
-Provides accurate and reliable results
-Can be measured indoors and outdoors as well
-Used for the accurate quantitative measurement of glucose (sugar) present in the blood
-The high-low alarm helps in giving the accurate information about one's blood glucose levels
-Each strip is meant to be used one-time use
-The device includes a lancing device, 10 strip lancets, owners guide, 1 case and 1 High--Low Alarm Reference Card
Directions For Use
Insert the strip to start and apply blood
Reading will appear on the screen
Safety Information:
- Read the label carefully before use
- Keep out of the reach of children
- Do not refrigerate
-Store in a cool dry place
-Do not use if the expiry date has passed
-To be used within 6 months of opening the test strip vial
The Accu-Chek® Instant S blood glucose monitoring system helps to lower the testing barriers by supporting the ease-of-use with its components and features: TRI tool and USB connectivity to the Accu-Chek® Connect Online system.
Instant clarity
Get Instant clarity of your results in just a few seconds with a visual re-assurance. The intuitive 9 colour target range indicator helps you understand your results easily and know if they are above, in range or below range.
Proven accuracy
Guaranteed by the makers of the Accu-Chek products, fulfilling the requirements of the ISO 15197: 2013^ and delivering even tighter accuracy for reliable results you can trust.
1 button navigation
Only what you need: Your test result and your averages (7/30/90 days) are visible on the meter.
So there is no need to scroll through a menu to find what you need. 1 button is all it takes.
No set up
Simple preparation: No set up required â� just insert a strip, apply a small blood sample, and read your blood glucose result on the large display. Remove the test strip after testing and the meter turns off automatically.
Blood application
Easy-edge blood dosing: A small blood sample can be applied anywhere on the wide, yellow edge of the test strip dosing area, that has a wide blood application area compared to leading brands.
The test strip is designed to help make it easy to apply a small drop of blood on the end of the strip.
* Blood glucose values (Lowsâ?¤69mg/dL, Normal 70-160 mg/dL, Highâ?¥161/dL) are pre-set on the Target Range Indicator and must be interpreted in conjunction with the appropriate medical condition at the time of taking reading, and in accordance with advice of your physician.
^ Criterion A of clause 6.3 for the lot tested (Freckmann et al., JDST, 6(5), 2012)
# Figures refer to the TRI tool group of the study (n = 47)
1 Parkin CG, et al. Use of an Integrated Tool for Interpretation of Blood Glucose Data Improves Correctness of Glycemic Risk Assessment in Individuals With Type 1 and
Type 2 Diabetes. J Diabetes Sci Technol
Accu-Chek Active Strip helps in determining the blood sugar level in the body. The sugar test strips absorb the blood easily and spreads quickly on the strip. The strips need a small amount of blood that shows reliable results in a few seconds. The kit includes Accu-Chek Active strips that can be used until the expiration date printed on the pack. After the test matches the colour of the strip visually to the closest coloured dot on the test strip container. The Acc-Chek strips are available in packs of 10, 25 and 50 strips.
Benefits and Features
accurate:
Accurate1 blood glucose measurement
easy:
- No coding for even easier blood glucose monitoring
- easy-to-read display (new typeface)
- intuitive handling with just 2 buttons
safe:
- Underdose detection
- visual double check
- 10 seconds re-dose option
clever:
- Pre- and postmeal markers
- postprandial reminder
- 7,14,30 or now 90 day test averages
- USB interface for data transfer
With XIENCE Sierra's new stent design, the XIENCE reputation now extends to offer unmatched deliverability, even with challenging complex lesions.
ULTRA LOW STENT CROSSING PROFILE1 OF 0.039â?³
FOR EASIER CROSSING
enabled by the new stent design and balloon technology1
XIENCE Sierra's exceptional deliverability also comes from the enhanced stent delivery system featuring a single-piece outer member for added pushability and trackability.
Expanded Treatment Optionsâ?¡
With 5.5 mm post-dilatation capability for 3.5 mm and 4.0 mm stents, XIENCE Sierra can treat most large vessels.
PROVIDES UNSURPASSED PRECISION IN PLACEMENT AND AVOID GEOGRAPHIC MISS
zero shortening even at max expansion of 5.5 mm2
XIENCE SIERRA ENSURES COATING INTEGRITY3
even at max expansion
XIENCE Sierra
coating remains intact at maximum post-dilatation expansion
of 5.5 mm from 3.5 mm
XIENCE Sierra (3.5 x 18 mm)
25x magnification at max expansion
of 5.5 mm
XIENCE Sierra (3.5 x 18 mm)
150x magnification at max expansion
of 5.5 mm
Synergy
coating shows multiple cracks with delamination at its max
expansion of 4.25 mm from 3.5 mm
Xience Xpedition represents a powerful combination of deliverability, strong clinical data and broad availability of meaningful sizes, three factors that make this product well-suited to treat a wide range of patients, The impact of the changes to the stent delivery system is particularly notable in patients with complex coronary anatomy. For these patients, physicians have a new technology to reach the blockage and restore blood flow with ease and confidence. In order to cater the variegated demands of our beloved clients, we are offering a wide range of Abbott Xience Xpedition Stent
The Endo Bag single-use specimen container is supplied sterile in a dispensing tube for ease of insertion through a standard 10 mm, 11 mm, or 12 mm trocar cannula.
Currently marketed specimen retrieval bags differ in their size (i.e., diameter of the bag) and in the technique employed to open and deploy the bag. The most commonly used specimen bags in gynecology range from 10 to 15 cm in diameter, and allow for easy removal of most adnexal masses. The 10 cm bags usually require a 10 mm laparoscopic port for introduction into the abdomen, which may be placed in the umbilicus or in the lower abdomen. The advantage of using a 10 cm umbilical port for introduction of the bag instead of a lower abdominal port is that the former usually does not require fascial closure. The 15 cm specimen bag usually requires a 12 mm port for introduction into the pelvic, necessitating closure of the fascia layer to avoid port-site hernia.
Specimen retrieval bags also differ in their opening technique. Some specimen bags have the ability to open automatically after introduction into the abdomen, while others require manual opening by two graspers holding the bag edges. The bags with automatic opening are usually easier to use, but often more expensive than the bags with manual opening an automatically opening bag (Endocatch, manufactured by Covidien, Mansfield, MA, USA), respectively. All bags are manufactured for single use. We have found that the specimen bag with a 10-cm diameter and manual opening is suitable for most adnexal surgeries, obviating the need to use the more expensive bags with automatic opening Some authors have described the use of home-made specimen bags, such as a surgical glove or a zipper storage bag, which are cheaper than the manufactured bags
GST60G ECHELON ENDOPATH
Control Tissue Slippage During Firing
4x less tissue slippage for the most precise transection. Uniquely designed for better grip to provide the least tissue slippage§ for the most precise transection. Proprietary Gripping Surface Technology provides superior tissue grip without additional trauma during firing. This means you can transect more of the tissue you intended - especially in very thick tissue - with each firing.
GST60B ETHELON
Control Tissue Slippage During Firing
4x less tissue slippageâ? for the most precise transection. Uniquely designed for better gripâ?¡ to provide the least tissue slippage§ for the most precise transection. Proprietary Gripping Surface Technology provides superior tissue gripâ without additional trauma during firing. This means you can transect more of the tissue§ you intended - especially in very thick tissue - with each firing.
Description
60mm Green Reload
Brand
ECHELON ENDOPATH
Staple Technology
B-Form
Device Technology
Natural Articulation
Size
60mm
Color
GREEN
Staple Rows
6
Tissue Thickness
Thick
Open Staple Height
4.1mm
Closed Staple Height
2.0mm
Category
Surgical Stapling
QTY/BX
12
Description
60mm Green Reload
Brand
ECHELON ENDOPATH
Staple Technology
B-Form
Device Technology
Natural Articulation
Size
60mm
Color
GREEN
Staple Rows
6
Tissue Thickness
Thick
Open Staple Height
4.1mm
Closed Staple Height
2.0mm
Category
Surgical Stapling
QTY/BX
12
Description
60mm Gold Reload
Brand
ECHELON ENDOPATH
Staple Technology
B-Form
Device Technology
Natural Articulation
Size
60mm
Color
Gold
Staple Rows
6
Tissue Thickness
Regular/Thick
Open Staple Height
3.8mm
Closed Staple Height
1.8mm
Category
Surgical Stapling
QTY/BX
12
ADVAPD Suture is synthetic absorbable sterile surgical suture composed of a copolymer made from polyester and Polydioxanone.
The advanced extrusion process of the molecule of Polydioxanone gives ADVAPD:
ADVAPD Suture is indicated for use in soft tissue approximation, including use in pediatric cardiovascular tissue where growth is expected to occur and ophthalmic surgery. PDS II Suture is not indicated in adult cardiovascular surgery, microsurgery and neural tissue.
ADVAPD Suture is particularly useful where the combination of an absorbable suture and extended wound support (up to six weeks) is desirable.
ADVAPD Suture, being absorbable, is not to be used where prolonged (beyond six weeks) approximation of tissues under stress is required and is not to be used in conjunction with prosthetic devices (i.e. heart valves or synthetic grafts). Suture absorption occurs by means of hydrolysis. Absorption begins as a loss of tensile strength followed by a loss of mass.
ADVALON Suture is indicated for use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurological procedures.
ADVALON Suture elicits a minimal acute inflammatory reaction in tissue, which is followed by a gradual encapsulation of the suture by fibrous connective tissue. While nylon is not absorbed, progressive hydrolysis of the nylon in vivo may result in gradual loss of tensile strength over time.
Due to the gradual loss of tensile strength which may occur over prolonged periods in vivo, nylon suture should not be used where permanent retention of tensile strength is required.
Features
Benefits
Excellent pliability
Provides exceptional handling and knot tying properties
Monofilament construction
Easy passage through tissue with low frictional co-efficient
Inert polymer
Ideal for infected wound closure Suture of choice for desired cosmetic outcomes
Excellent elasticity
Superior tactile feedback to the surgeon, minimal suture breakage
Tyvek packaging
Durable protection & long lasting sterility
Gamma radiation of sterilization
Environmental friendly & less hazardous
300 Series premium cutting needles
Strong & sharp needles for minimal bending & desired cosmetic outcomes
Durable silicon coated needles
Significantly enhanced initial and multi-pass penetration
Ribbed bodied needles
Better grasping & superior needle control
ADVACRYL Suture is synthetic absorbable sterile surgical suture composed of a copolymer made from 90% Glycolide and 10% L-lactide. Braided ADVACRYL Suture is coated with a mixture composed of Poly (Glycolide-co-lactide) (Glacomer 37) and calcium stearate. The suture is colored violet to increase visibility and is also available undyed.
The advanced extrusion process of copolymer, the exclusive braiding process and coating system, give ADVACRYL:
ADVACRYL Suture is indicated for use in general soft tissue approximation and/or ligation, including use in ophthalmic procedures, but not for use in cardiovascular and neurological tissues.
ADVACRYL Suture being absorbable, should not be used where permanent support of tissue is required.
Progressive loss of tensile strength and eventual absorption of ADVACRYL Suture occurs by means of hydrolysis. Absorption begins as a loss of tensile strength followed by a loss of mass.
ADVALENE Suture is non-absorbable, sterile surgical suture composed of an isotactic crystalline stereoisomer of polypropylene. The suture is coloured blue to enhance visibility.
The advanced extrusion process of the polypropylene molecule gives ADVALENE:
ADVALENE Suture is indicated for use in general soft tissue approximating and/or ligation, including use in cardiovascular, ophthalmic procedures, and neurological procedures.
ADVALENE Suture complies with united state pharmacopeia requirement for Non- absorbable surgical suture.
ADVALENE Suture elicit a minimal inflammatory reaction in tissue, which is followed by gradual encapsulation of the suture by fibrous connective tissue. ADVALENE Suture is not absorbed, nor is they subject to degradation or weakening by the action of tissue enzymes.
As a monofilament, ADVALENE Suture is inert, resist involvement in infection and have been successfully employed in contaminated and infected wounds to eliminate or minimize later sinus formation and suture extrusion.
Furthermore, the lack of adherence to the tissues has facilitated the use of ADVALENE Suture as a pull-out suture.
ADVASYL Suture is indicated for use in general soft tissue approximating and/or ligation, including use in cardiovascular, ophthalmic, and neurological procedures.
ADVASYL Suture elicits an acute inflammatory reaction in tissue, which is followed by a gradual encapsulation of the suture by fibrous connective tissue. While silk is not absorbed, progressive degradation of the proteinaceous silk fiber in vivo may result in gradual loss of all of the sutures tensile strength overtime.
Company Information
Lakshay Surgicals, established in 2012, is engaged in the business of manufacturer, exporter, wholesaler and trader of superlative quality Medical Equipments. The offered equipment is engineered in accordance with the industry set norms using good quality metal. Offered range of products includes Diagnostic Equipment, Front Loading Autoclave Enclaves and ENT Products. Extremely demanded in hospitals, nursing homes and health clinics, our products are praised for their perfect finishing, light weight, optimum functionality and high durability. Furthermore, offered equipment is made available at market leading prices. We export our products in all over the world.
To offer unmatched quality medical equipment to our esteemed customers, we have hired a team of efficient quality controllers. These products are engineered in accordance with the parameters decided by our quality controllers. Before the final dispatch, offered products are stringently examined by the controllers on various parameters. Owing to the assistance of our trustworthy logistic partners, we deliver these products promptly. Besides, our flexible payment options place us among the prominent names in this domain.
NEW XIENCE SIERRA STENT DESIGN
The new XIENCE Sierra Stent Design, with Slim Flex Technology, has a lower crossing profile1 and greater post-dilatation expansion
NEW STENT DELIVERY SYSTEM FOR COMPLEX CASES
Design innovations built to provide the flexibility, crossability, and pushability needed for even the most complex cases.
The XIENCE V®, XIENCE nano®, XIENCE PRIME®, XIENCE PRIME® LL, XIENCE Xpedition®, XIENCE Xpedition® SV and XIENCE Xpedition® LL , XIENCE Alpine®, and XIENCE SierraTM (XIENCE Family) of Everolimus Eluting Coronary Stents on the MULTI-LINK VISION® or MULTI-LINK MINI VISION® Delivery System
INDICATIONS
The XIENCE Sierra stent system is indicated for improving coronary artery luminal diameter in patients, including those with diabetes mellitus, with symptomatic heart disease due to de novo native coronary artery lesions (length â?¤ 32 mm) with reference vessel diameters of â?¥ 2.25 mm to â?¤ 4.25 mm. In addition, the XIENCE Sierra stent system is indicated for treating de novo chronic total coronary occlusions.
CONTRAINDICATIONS
The XIENCE Sierra stent system is contraindicated for use in:
Patients who cannot tolerate, including allergy or hypersensitivity to, procedural anticoagulation or the post-procedural antiplatelet regimen.
Patients with hypersensitivity or contraindication to everolimus or structurally related compounds, or known hypersensitivity to stent components (cobalt, chromium, nickel, tungsten, acrylic, fluoropolymers), or with contrast sensitivity.
WARNINGS
It is not recommended to treat patients having a lesion that prevent complete inflation of an angioplasty balloon.
Judicious patient selection is necessary because the use of this device carries the associated risk of stent thrombosis, vascular complications, and/or bleeding events.
This product should not be used in patients who are not likely to comply with the recommended antiplatelet therapy.
The second-generation Xience V everolimus-eluting stent incorporates advanced design features such as a cobalt-chromium stent platform coated with an antirestenotic drug, everolimus, incorporated into a biocompatible polymer with a long history of medical use. The efficacy of the stent has been demonstrated with low rates of angiographic restenosis, whilst randomized trials comparing the Xience V everolimus-eluting stent to the first-generation Taxus paclitaxel-eluting stent have found a reduction in repeat revascularization rates. Further randomized trials, including 'all-comer' patients and registries of unselected patients are currently further evaluating the efficacy and safety of the Xience V stent in high-risk, complex cases.We also offer one of the most primary quality stents in the market, The Xience V Stent
Coronary artery stents are devices (small metallic mesh tubes) that are placed over a balloon catheter and delivered to the narrowed portion of the coronary artery. The balloon is used to expand the stent. The stent presses against the narrowed vessel wall, holding the vessel open. This results in a wider artery channel to improve blood flow to the heart muscle. This may be followed by repeat balloon inflations within the stent to achieve the result desired by your doctor. Once the balloon has been deflated and withdrawn, the stent stays in place permanently, holding the coronary artery open. The inner lining of the artery grows over the surface of the stent, making the stent a permanent part of your artery
Description
60mm Gold Reload
Brand
ECHELON ENDOPATH
Staple Technology
B-Form
Device Technology
Natural Articulation
Size
60mm
Color
White
Staple Rows
6
Tissue Thickness
Regular/Thick
Open Staple Height
3.8mm
Closed Staple Height
1.8mm
Category
Surgical Stapling
QTY/BX
12
PROLENEâ?¢ Polypropylene Mesh is constructed of knitted filaments of extruded polypropylene identical in composition to that used in PROLENEâ?¢ Polypropylene Suture, Nonabsorbable Surgical Sutures, U.S.P. (Ethicon, LLC). The mesh is approximately 0.020 inches thick. This material, when used as a suture, has been reported to be nonreactive and to retain its strength indefinitely in clinical use. PROLENE Mesh is knitted by a process which interlinks each fiber junction and which provides for elasticity in both directions. This construction permits the mesh to be cut into any desired shape or size without unraveling. The fiber junctions are not subject to the same work fatigue exhibited by more rigid metallic meshes. This bi-directional elastic property allows adaption to various stresses encountered in the body.
Abbott BMW Guide Wire with hi-torque balance middleweight universal guide wire is a front-line guide wire offering a unique balance of support and flexibility, with enhancements in the areas of device compatibility, distal access, deliverability in tortuous anatomy and tip durability.
INDICATIONS FOR USE
This HI-TORQUE Guide Wire is intended to facilitate the placement of balloon dilatation catheters during Percutaneous Transluminal Coronary Angioplasty (PTCA) and Percutaneous Transluminal Angioplasty (PTA). This guide wire may also be used with compatible stent devices during therapeutic procedures.
CONTRAINDICATIONS
Not intended for use in the cerebral vasculature or with atherectomy devices.
WARNINGS
This device is designed and intended for ONE-TIME USE ONLY. Do not resterilize and / or reuse.
Carefully observe the instructions under Do Not and Do below. Failure to do so may result in vessel trauma, guide wire damage, guide wire tip separation, or stent damage. If resistance is observed at any time, determine the cause under fluoroscopy and take remedial action as needed. Use the most suitable guide wire for the lesion being treated.
Guide wires with a high manoeuvrability in the chronic occluded lesion, and a tip designed to improve penetrability into the lesion while remaining flexible.
Features
0.014" Guide wire
Tapered tip options, 0.010" (1.7gf wire), 0.011" (3.5gf wire) and 0.012" (4.5gf wire)
1.7gf, 3.5gf and 4.5gf Tip load options
1:1 Torque
40cm Hydrophilc coating
15cm Spring coil length
15cm Radiopaque segment
Available in 190cm and 300cm lengths
