Articsun Arctic Gel Pads Large Kit REF 317-09 EXP. 2012-09 In original factory packaging & never opened May be non-sterile due to expiration date Single patient use. New in original unopened factory package. Units are sold as non-sterile due to expiration of packaging. See pictures for more information. Not for human consumption. Not an implantable device. Items sold a non-sterile due to expiration of sterility on packaging are sold as-is and may be re-sterilized and used for training or veterinary purposes. "The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. Do not purchase this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item." DISCLAIMER: Regardless of the origin of the equipment, documentation provided or identification appearing upon the equipment, the equipment described and offered here is in no way certified for, recommended for, or offered for any specific use. The purchaser agrees that the seller shall not be held responsible or liable for any injuries or damages, whether incidental or consequential, associated in any way with the equipment. The purchaser, by purchasing this equipment, indicates their acknowledgment of, and agreement to the terms of this disclaimer. WAIVER LIABILITY AND INDEMNIFICATION AGREEMENT By placing this order with THE SELLER of this sale and accepting the parts, the purchaser agrees that the purchased materials or parts will be used solely at the purchaser's risk and that the purchaser will indemnify and hold THE SELLER, its owners and employees, free and harmless from all loss, liability and damage resulting from claims brought by any regulatory agencies, or by reason of any alleged failure or defect of any parts supplied by THE SELLER.
Fisher & Paykel Bi-Level CPAP Full Face Mask and Headgear 1 - REF RT040S EXP. 2010-07 5 - REF RT040M EXP. 2011-08 7 - REF RT040L EXP. 2011-10 In original factory packaging & never used May be non-sterile due to expiration date Single patient use. New in original unopened factory package. Units are sold as non-sterile due to expiration of packaging. See pictures for more information. Not for human consumption. Not an implantable device. Items sold a non-sterile due to expiration of sterility on packaging are sold as-is and may be re-sterilized and used for training or veterinary purposes. "The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. Do not purchase this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item." DISCLAIMER: Regardless of the origin of the equipment, documentation provided or identification appearing upon the equipment, the equipment described and offered here is in no way certified for, recommended for, or offered for any specific use. The purchaser agrees that the seller shall not be held responsible or liable for any injuries or damages, whether incidental or consequential, associated in any way with the equipment. The purchaser, by purchasing this equipment, indicates their acknowledgment of, and agreement to the terms of this disclaimer. WAIVER LIABILITY AND INDEMNIFICATION AGREEMENT By placing this order with THE SELLER of this sale and accepting the parts, the purchaser agrees that the purchased materials or parts will be used solely at the purchaser's risk and that the purchaser will indemnify and hold THE SELLER, its owners and employees, free and harmless from all loss, liability and damage resulting from claims brought by any regulatory agencies, or by reason of any alleged failure or defect of any parts supplied by THE SELLER.
Lot of 9 DeRoyal St. Shoulder Suspension Kits REF 32-525 EXP. 2012-09 In original factory packaging & never opened May be non-sterile due to expiration date isclaimer Single patient use. New in original unopened factory package. Units are sold as non-sterile due to expiration of packaging. See pictures for more information. Not for human consumption. Not an implantable device. Items sold a non-sterile due to expiration of sterility on packaging are sold as-is and may be re-sterilized and used for training or veterinary purposes. "The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. Do not purchase this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item." DISCLAIMER: Regardless of the origin of the equipment, documentation provided or identification appearing upon the equipment, the equipment described and offered here is in no way certified for, recommended for, or offered for any specific use. The purchaser agrees that the seller shall not be held responsible or liable for any injuries or damages, whether incidental or consequential, associated in any way with the equipment. The purchaser, by purchasing this equipment, indicates their acknowledgment of, and agreement to the terms of this disclaimer. WAIVER LIABILITY AND INDEMNIFICATION AGREEMENT By placing this order with THE SELLER of this sale and accepting the parts, the purchaser agrees that the purchased materials or parts will be used solely at the purchaser's risk and that the purchaser will indemnify and hold THE SELLER, its owners and employees, free and harmless from all loss, liability and damage resulting from claims brought by any regulatory agencies, or by reason of any alleged failure or defect of any parts supplied by THE SELLER.
Lot of 30 Portex Face Masks (Adult Medium Hook Ring Valve) REF 005445 EXP. 2017-09 In original factory packaging & never opened Single patient use. New in original unopened factory package. See pictures for more information. Not for human consumption. Not an implantable device. "The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. Do not purchase this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item." DISCLAIMER: Regardless of the origin of the equipment, documentation provided or identification appearing upon the equipment, the equipment described and offered here is in no way certified for, recommended for, or offered for any specific use. The purchaser agrees that the seller shall not be held responsible or liable for any injuries or damages, whether incidental or consequential, associated in any way with the equipment. The purchaser, by purchasing this equipment, indicates their acknowledgment of, and agreement to the terms of this disclaimer. WAIVER LIABILITY AND INDEMNIFICATION AGREEMENT By placing this order with THE SELLER of this sale and accepting the parts, the purchaser agrees that the purchased materials or parts will be used solely at the purchaser's risk and that the purchaser will indemnify and hold THE SELLER, its owners and employees, free and harmless from all loss, liability and damage resulting from claims brought by any regulatory agencies, or by reason of any alleged failure or defect of any parts supplied by THE SELLER.
Lot of 10 Arrow Super Arrow-Flex Percutaneous Sheath Introducer Kit REF CP-07511-P EXP. 2012-07 In original factory packaging & never opened May be non-sterile due to expiration date Single patient use. New in original unopened factory package. Units are sold as non-sterile due to expiration of packaging. See pictures for more information. Not for human consumption. Not an implantable device. Items sold a non-sterile due to expiration of sterility on packaging are sold as-is and may be re-sterilized and used for training or veterinary purposes. "The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. Do not purchase this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item." DISCLAIMER: Regardless of the origin of the equipment, documentation provided or identification appearing upon the equipment, the equipment described and offered here is in no way certified for, recommended for, or offered for any specific use. The purchaser agrees that the seller shall not be held responsible or liable for any injuries or damages, whether incidental or consequential, associated in any way with the equipment. The purchaser, by purchasing this equipment, indicates their acknowledgment of, and agreement to the terms of this disclaimer. WAIVER LIABILITY AND INDEMNIFICATION AGREEMENT By placing this order with THE SELLER of this sale and accepting the parts, the purchaser agrees that the purchased materials or parts will be used solely at the purchaser's risk and that the purchaser will indemnify and hold THE SELLER, its owners and employees, free and harmless from all loss, liability and damage resulting from claims brought by any regulatory agencies, or by reason of any alleged failure or defect of any parts supplied by THE SELLER.
Vertical fold-flat, without exhalation valve Welded elastic earloops Imbedded nose clip, sponge nose lining CE approved by UNIVERSAL (NB no. 2163) Tested and certified according to EN 149:2001+A1:2009 Class: FFP3 NR This respirator mask is certified and classified as FFP3 under EU standard EN 149:2001+A1:2009. EN 149:2001+A1:2009 - Respiratory protective devices - Filtering half masks to protect against particles. This European Standard specifies the minimum requirements for filtering half masks used as respiratory protective devices, specifically against particles, and the required laboratory and practical performance tests to assess masks' compliance. EN 149:2001+A1:2009 classified half masks into three types according to their filtering capacities: FFP1, FFP2 and FFP3. Respirators that meet the requirements of EN 149:2001+A1:2009 are designed to protect against solids, water-based aerosols, and oil-based aerosols. FFP3 masks have a minimum of 99% filtration percentage and maximum 2% leakage to the inside. They are mainly used in construction, agriculture, and by healthcare professionals against influenza viruses.
Vertical fold-flat, without exhalation valve Welded elastic earloops Imbedded nose clip, sponge nose lining CE approved by UNIVERSAL (NB no. 2163) Tested and certified according to EN 149:2001+A1:2009 Class: FFP3 NR This respirator mask is certified and classified as FFP3 under EU standard EN 149:2001+A1:2009. EN 149:2001+A1:2009 - Respiratory protective devices - Filtering half masks to protect against particles. This European Standard specifies the minimum requirements for filtering half masks used as respiratory protective devices, specifically against particles, and the required laboratory and practical performance tests to assess masks' compliance. EN 149:2001+A1:2009 classified half masks into three types according to their filtering capacities: FFP1, FFP2 and FFP3. Respirators that meet the requirements of EN 149:2001+A1:2009 are designed to protect against solids, water-based aerosols, and oil-based aerosols. FFP3 masks have a minimum of 99% filtration percentage and maximum 2% leakage to the inside. They are mainly used in construction, agriculture, and by healthcare professionals against influenza viruses.
FFP2 Vertical-Flat Respirator Face Mask CE certified by Universal Certification (NB no. 2163) Tested and certified according to EN 149:2001+A1:2009 Class: FFP2 This respirator mask is certified and classified as FFP2 under EU standard EN 149:2001+A1:2009. EN 149:2001+A1:2009 - Respiratory protective devices - Filtering half masks to protect against particles. This European Standard specifies the minimum requirements for filtering half masks used as respiratory protective devices, specifically against particles, and the required laboratory and practical performance tests to assess masks' compliance. EN 149:2001+A1:2009 classified half masks into three types according to their filtering capacities: FFP1, FFP2 and FFP3. Respirators that meet the requirements of EN 149:2001+A1:2009 are designed to protect against solids, water-based aerosols, and oil-based aerosols. FFP2 masks have a minimum of 94% filtration percentage and maximum 8% leakage to the inside. They are mainly used in construction, agriculture, and by healthcare professionals against influenza viruses.
FFP2 Vertical-Flat Respirator Face Mask CE certified by Universal Certification (NB no. 2163) Tested and certified according to EN 149:2001+A1:2009 Class: FFP2 This respirator mask is certified and classified as FFP2 under EU standard EN 149:2001+A1:2009. EN 149:2001+A1:2009 - Respiratory protective devices - Filtering half masks to protect against particles. This European Standard specifies the minimum requirements for filtering half masks used as respiratory protective devices, specifically against particles, and the required laboratory and practical performance tests to assess masks' compliance. EN 149:2001+A1:2009 classified half masks into three types according to their filtering capacities: FFP1, FFP2 and FFP3. Respirators that meet the requirements of EN 149:2001+A1:2009 are designed to protect against solids, water-based aerosols, and oil-based aerosols. FFP2 masks have a minimum of 94% filtration percentage and maximum 8% leakage to the inside. They are mainly used in construction, agriculture, and by healthcare professionals against influenza viruses.
FFP2 Vertical-Flat Valved Respirator Face Mask CE certified by CCQS Ireland (NB no. 2834) Tested and certified according to EN 149:2001+A1:2009 Module Type of Certification: Module B + Module C2 Class: FFP2 This respirator mask is certified and classified as FFP2 under EU standard EN 149:2001+A1:2009. EN 149:2001+A1:2009 - Respiratory protective devices - Filtering half masks to protect against particles. This European Standard specifies the minimum requirements for filtering half masks used as respiratory protective devices, specifically against particles, and the required laboratory and practical performance tests to assess masks' compliance. EN 149:2001+A1:2009 classified half masks into three types according to their filtering capacities: FFP1, FFP2 and FFP3. Respirators that meet the requirements of EN 149:2001+A1:2009 are designed to protect against solids, water-based aerosols, and oil-based aerosols. FFP2 masks have a minimum of 94% filtration percentage and maximum 8% leakage to the inside. They are mainly used in construction, agriculture, and by healthcare professionals against influenza viruses.
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
Lot of 12 Various Kits 1 Arrowgard Blue Large-Bore Multi-Lumen CVC Kit REF. CDC-22123-1A EXP. 2013-08 1 Pneumothorax Kit REF. AK-01500 EXP. 2013-03 1 Pressure Injectable Multi-Lumen CVC Kit REF. CDC-15703-P1A EXP. 2013-10 1 Large-Bore Multi-Lumen CVC Kit REF. CDC-25123-1A EXP. 2012-10 2 Arterial Line Kits REF. AK-04510-S EXP. 2013-03 2 Radial Artery Catheterization Kits REF. AK-04020 EXP. 2013-07 4 Pediatric Multi-Lumen Central Venous Catheterization Set REF. CS-16553-J EXP. 2013-01 isclaimer Single patient use. New in original unopened factory package. Units are sold as non-sterile due to expiration of packaging. See pictures for more information. Not for human consumption. Not an implantable device. Items sold a non-sterile due to expiration of sterility on packaging are sold as-is and may be re-sterilized and used for training or veterinary purposes. "The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. Do not purchase this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item." DISCLAIMER: Regardless of the origin of the equipment, documentation provided or identification appearing upon the equipment, the equipment described and offered here is in no way certified for, recommended for, or offered for any specific use. The purchaser agrees that the seller shall not be held responsible or liable for any injuries or damages, whether incidental or consequential, associated in any way with the equipment. The purchaser, by purchasing this equipment, indicates their acknowledgment of, and agreement to the terms of this disclaimer. WAIVER LIABILITY AND INDEMNIFICATION AGREEMENT By placing this order with THE SELLER of this sale and accepting the parts, the purchaser agrees that the purchased materials or parts will be used solely at the purchaser's risk and that the purchaser will indemnify and hold THE SELLER, its owners and employees, free and harmless from all loss, liability and damage resulting from claims brought by any regulatory agencies, or by reason of any alleged failure or defect of any parts supplied by THE SELLER.
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 skid-mate is an air dampened cushioning device that provides a fast, cost effectiveand durable customized solution to protect sensitive products from shock and vibration. Theskid-mate can be easily mounted on a crate or pallet base creating an air-ride cushion in placeof hardwood skid runners eliminating the need for expensive air-ride trucks.Each color coded skid-mate corresponds to a specific load range and allows users to calculatetheir requirements simply and easily to avoid potential laboratory testing and use of expensivepackaging materials. Reduce packaging design & assembly time and cost• eliminate costly damage from handling hazards during shipment• reduce costs associated with shock and vibration damage
A golf course sand consists of a series of holes, each consisting of a teeing ground, fairway, rough and other hazards, and a green with a flagstick (pin) and cup, all designed for the game of golf. A standard round of golf consists of playing 18 holes, thus most golf courses have this number of holes.] Some, however, only have nine holes, and the course is played twice per round (2×9=18), while others have 27 or 36 holes and choose two groups, of nine holes at a time, for novelty and maintenance reasons. Additionally, par-3 courses also exist, consisting of nine or 18 holes, all of which are a par 3 (strokes for a scratch golfer). Many older golf courses, often coastal, are golf links, of a different style to others. For non-municipal courses, there is usually a golf club based at each course, and may include a pro shop. USGA Test Analysis USGA Specification Of Silica Sand For The Use On Golf Green Construction A. We produce and supply different colors of sand according to USGA B. Our Golf Course Sand Has Two Different Varieties C. White quartz silica sand with high purity more than 99.3% D. Second variety with yellowish color with purity 96.7 E. Origin: EGYPT F. Packing can be customized according to buyer request G. Can be bulk by trucks, bulk be vessel, bags of 1500kg H. Large quantities can be arranged I. High daily productivity with our own screening plant J. Quality control for each batch on our site lab by sieving test analysis
golf course sand A golf course sand consists of a series of holes, each consisting of a teeing ground, fairway, rough and other hazards, and a green with a flagstick (pin) and cup, all designed for the game of golf. A standard round of golf consists of playing 18 holes, thus most golf courses have this number of holes.] Some, however, only have nine holes, and the course is played twice per round (2Ã??9=18), while others have 27 or 36 holes and choose two groups, of nine holes at a time, for novelty and maintenance reasons. Additionally, par-3 courses also exist, consisting of nine or 18 holes, all of which are a par 3 (strokes for a scratch golfer). Many older golf courses, often coastal, are golf links, of a different style to others. For non-municipal courses, there is usually a golf club based at each course, and may include a pro shop. USGA TEST ANALYSIS USGA SPECIFICATION OF SILICA SAND FOR THE USE ON GOLF GREEN CONSTRUCTION We produce and supply different colors of sand according to USGA OUR GOLF COURSE SAND HAS TWO DIFFERENT VARIETIES White quartz silica sand with high purity more than 99.3% Second variety with yellowish color with purity 96.7 Origin: EGYPT Packing can be customized according to buyer request Can be bulk by trucks, bulk be vessel, bags of 1500kg Large quantities can be arranged High daily productivity with our own screening plant Quality control for each batch on our site lab by sieving test analysis
Place of Origin: China Brand Name: OEM Model Number: DAT009 Power Source: Electric Warranty: 1 Year After-sale Service: Online technical support Material: Acrylic, Plastic Shelf Life: 1years Quality Certification: ce Instrument classification: Class I Safety standard: None Type: Pathological Analysis Equipments Product name: drug abuse test Format: Strip/Cassette Specimen: Urine MOQ: 20000 pieces for BUP drug test kits Test Items: BUP Storage time: 4â??-30â?? Detection time: 5min OEM: Acceptable Keywords: drug test
Product Price(FOB) - 0.45 USD per piece Product Origin - india Specification - "Compact design High durability Low maintenance Per Pcs ETO Sterelized MOQ & Packaging - 10,000 pieces
Specification:50ml,60ml,100ml Unique labeling urine collection hole makes urine collecting and transferring convenient sanitary and safe. This container can prevent outer substance and bacteria contaminating urine specimen and urine spilling, which maximally avoids the risk of contacting pathogenic urine specimen by patient and medial people. The label is easy to tear and re-seal. Packing:500pcs/ctn Weight:G.W.7.8kg/ctn, N.W.6.0kg/ctn Dimension:595mm*490mm*400mm
Product Features It is designed focus on system, which overcomes the shortcomings of poor systemicity of traditional products with a single device or component as the main design. Absorb the essence of domestic and foreign dosing technology, and optimize the process with a new design concept. Product structure modular design, integrated combination, can easily expand capabilities and functions. Flexible configuration of the best solution according to different water quality and different requirements of users. A variety of components comes from well-known brands at domestic and abroad, with different materials and grades, and be optional. � Applications: � Furnace water treatment system, circulating cooling system, central air conditioning circulating water system, raw water pretreatment and waste water treatment system in thermal power generation industry. Furnace water treatment system, circulating cooling system, chemical additive dosing system, medical treatment, electronics and other industries in the petroleum and chemical industry. Disinfection of municipal water supply, swimming pools, water plants, sewage treatment, building domestic water. Disinfection of industrial circulating water and industrial water treatment. Other related industry liquid dosing systems.
