Trophon Chemical Indicator Strip

KMNPack chemical indicator strips are manufactured in absence of lead or other heavy metals. They are constructed from special card, standard color patch and indicator strip. The process indicator ink shows clear and accurate color change and indicates if the pack has been processed.

KMNPack chemical&(Autoclave) steam indicator strips are manufactured in absence of lead or other heavy metals. They are constructed from special card, standard color patch and indicator strip. The process indicator ink shows clear and accurate color change and indicates if the pack has been processed.

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 ââ?¬ 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

General Description: Non-fluid resistant respirator mask protecting against airborne pathogens. Anti-penetration high filtration mask Technical specifications Product Name: FFP2 Respirator with harness band Material : 4-layer non-woven melt-blown fabric Bacteria Filtration level: > 94 % Air permeability: > 2 mm H2O Shape : foldable without valve Fits most face shapes, without inspiration/expiration air-leakage Adjustable nose bridge strip (4 x 90 mm (w x l) (+/-10%)) Elastic ear straps, both fitting around the ears or optional fitting around the top of the head with support of harness band(included). white colour Non-sterile Single-use, disposable Each mask bares clear identification of (i) protection provided FFP2, (ii) which side to wear up (nose), (iii) manufacturer's name, and (iv) model reference Conforms to standards: EN 149: 2001/FFP2. The disposable respirator should be marked with the manufacturer's name, EN 149: 2001/FFP2 and CE certification number. Certificate CE from notified body ISO13485 Supplied with Supplier's instruction for use Shelf life : As indicated by supplier Storage conditions: As indicated by supplier Packaging and labelling: Labelling of the primary packaging displays, at least: product name, product reference, manufacturer name, size, type and performance testing information against the mentioned standards. Information for particular storage conditions (temperature, pressure, light, humidity, etc.), as appropriate (or equivalent harmonised symbol), if applicable. All indicated at least in English

Product name: Coverall type 3B Elasticated hood around face. Elasticated cuffs and ankles. Elasticated sleeves. Taped seams. Zipper with re-sealable flap protecting leakage through seams. Stitched-in neck label indicating the type and performance of the suit against the below mentioned standards. White color with blue tape Material: 65 GSM Non-woven PP+PE 65 GSM +/- 2gsm Lightweight, do not contain rubber/ latex. Antistatic treated on both sides. Fabric is Infective agent tested against viral penetration at minimum 1.75kPa (class 2) (or equivalent international standard) Non-sterile Single Use, disposable Size: M-XL Conforms to standards below: European Directive 89/686/EEC on personal protective equipment Category III: Chemical protective coverall, comply with Type 4B/5B/6B including below standards. EN 13034:2005+A1 EN 14605 EN ISO 13982-1 EN 1073-2 EN ISO 13688 EN 1149-5 Barrier to infective agent standards: EN 14126:2003 certified passing infectious agent test according to ISO 16604:2004 (Resistance to penetration by bloodâ??borne pathogens using bacteriophage Phi X 174) standard at minimum exposure pressure of 1.75kPa (class 2) (or equivalent international standard) Performance requirement ISO standards: EN 340General requirements EN ISO 17491-4: 2008 (supersedes: EN 468 mod. â?? Spray aerosol test) EN 14325 Test methods & performance classification EN ISO 3758 (ISO 3758) Textile care symbols EN ISO 13935-2 Seam strength

INTENDED USE Giardia Ag Feces Rapid Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Giardia antigen in feces. Assay Time: 5-10 min Sample: Feces PRINCIPLE Giardia Ag Feces Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough Giardia antigen in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of Giardia antigen in the sample..