**Price update every week, for latest price contact** ** SGS inspection before payment release ** Product Description - Non-Sterile Powder-Free, Ambidextrous; Finger Tip Textured; Beaded Cuff, 100% nitrile - Certifications: CE, FDA 510(K),Conforms to ASTM D6319, ISO9001: 2008, ISO 13485:2003, ISO 22000:2005 - En455 Part 1-4 Tested TUV SUD - Packaging: 100 pcs in 1 box / 10 boxes in 1 carton - Sizes available: Extra-small, Small, Medium, Large, Extra-large
**Price update every week, for latest price contact** LC payment - $6.5-6.7 / box Ready Stock - $6.9 / box (MOQ: 5 million boxes) ** SGS inspection before payment release ** PRODUCT DESCRIPTION: Powder-free nitrile examination gloves, designed for both medical and food use. The gloves are ambidextrous and tested for use with chemotherapy drugs.100% Nitrile. CERTIFICATES: US FDA (510k) CE ASTM D6319, ASTM D6978 (Chemotherapy) ISO 13485:2016, ISO 9001-2015 EN ISO 374-1:2016, EN ISO 374-2:2014, EN ISO 374-4:2013, EN ISO 374-5:2016 EN420:2003+A1:2009 AQL 1.5 Packaging: 100 pcs in 1 box / 10 boxes in 1 carton Sizes available: Extra-small, Small, Medium, Large, Extra-large
**Price update every week, for latest price contact** Skymed non-sterile nitrile Examination gloves disposable medical gloves CE FDA certificated All the payments and contract with the Skymed OEM factory (Sufficiency Economy Co. Ltd.). 30% TT (advance) + 70% LC (on sight) ** SGS inspection will be provided before 70% payment release ** Minimum Order Quantity: 2 million boxes (pre-order) PRODUCT DESCRIPTION: - Powder Free, 100% Nitrile, Non- sterile, Ambidextrous, Beaded Cuff, Smooth/ textured finger tips - Certificates: FDA 510(K), EN455 Part 1-3, ASTM - D3578 - 01 - ae2, CE Packaging: 100 pcs in 1 box / 10 boxes in 1 carton Sizes available: Extra-small, Small, Medium, Large, Extra-large
Ready Stock Minimum Order Quantity - 5 million boxes PRODUCT DESCRIPTION: GloveOn COATS (Colloidal Oatmeal System) is a patented and unique nitrile glove technology, which contains an FDA-recognized skin protectant. STANDARDS FDA 510(k), CE, ASTM D6319, EN455 part 1, 2, 3 & 4, EN 1186, EN 13130, CEN/TS 14234, EN 420, EN 374 part 1 & 2 PACKAGING 100 gloves per box | 10 boxes per carton SIZES XS to XL
**Price update every week, please contact for latest price** Payment terms : LC/Escrow Quality Standard : - CE, FDA - Conforms to ASTM D6319 and EN 455 Standards. - Manufactured under QSR (GMP), ISO 9001:2008 & ISO 13485:2003 (Medical Device) Quality Management System. Product Description: - Non-Sterile Powder-Free, Ambidextrous; Finger Tip Textured; Beaded Cuff, 100% nitrile Packaging: 100 pcs in 1 box / 10 boxes in 1 carton Sizes available: Extra-small, Small, Medium, Large, Extra-large
Hand sterilizer drom South Korea 1. Alcohol 70% 2. USA FDA Certificate 3. Korean FDA Certificate(Quasi-drug) 4. Aloebera, Glycerin 5. Hydrating 6. No Harmful ingredients to the human body 7. Gel type, 500ml, 60ml, 30ml, & Pouch type 8. Container 20ft 16,000ea, 40ft 32,000 ea 9. Payment : 50% T.T, 50% L.C 10. Contact to me P.M
* Buyer issue LoI and BCL (current date ) *Every agent sign NCNDA and IMFPA * Seller issue soft corporate offer , which buyer need to sign and return within 2 calendar days * Buyer issue irrevocable purchase order * Seller issue full corporate offer , which buyer need to sign and return within 2 calendar days * Buyer issue RWA along with official draft of LC . * Seller issue draft of sales and purchase agreement on basis of ICPO and FCO and LC draft . * Buyer need to respond seller with in 2 calendar days and both party sign the agreement * Buyer issue LC , NOTE * LC should be from world top 10 bank. * Instrument should irrevocable , conformed , divisible , made by full cash deposit which will be payable against presentation of all documents as per agreement and LC. * Seller delivered material as per schedule confirmation in agreement. * Current allocation may vary and it depends when the seller gets LC stage. * Seller will not hold the schedule/stock until the instrument of the buyer not get confirm by the sellers banker officially.
Latex Examination Gloves Style: Disposable Certification: CE And FDA Sizes: All Quantity Required: 1 x 40-Foot Container Shipping Terms: CIF Destination Payment Terms: L/C or T/T Origin: Vietnam, Thailand, Malaysia Packing: 100 pics/ box, 10 boxes per carton
We, IREC GROUP and IREC GLOVE INDUSTRY (THAILAND) CO., LTD. hereby state that we own and hold the commercial rights of the ACCULYNE�® GLOVES brand of nitrile gloves. and can provide all necessary legal certifications/documents for export-import, sales and warranty. It is recognized and used by countries/states/countries around the world.
The ACCULYNE Nitrile Examination gloves are high performing 0.07 mm thickness powder-free blue coloured ambidextrous gloves that are intended for use in medical field to: protect patient and user from cross contamination, conducting medical examinations, diagnostic and therapeutic procedures and for handling medical contaminated material. This examination glove product conforms under International, American and European standards specific to: FDA device list code LZA, ASTM D6319-10, ASTM D6978-05, EN ISO 16523, EN 21420, EN374 and EN455. Materials Pure - Nitrile Type - Latex-Free, Odour-Free and Powder-Free Surface Treatments - Polymer Coated Colour - Light Blue Characteristics - Acrylonitrile Butadiene Rubber Sterilization = Non Sterlie Ambidextrous Beaded Cuf Use - Single use only Key Features Latex-Free 100% Nitrile Anti-static, surface resistance 109 ohms Powder Free Beaded Cuff Fully textured finger tips 3X Puncture Resistance of vinyl or latex gloves Pack: 100 gloves/dispenser boxes Industrial Applications Assembly Inspection Medical Dental Surgical Laboratory/ EMS Pharmaceutical manufacturing Painting and fishing Food processing/packing Cleaning
This kit is only used for the in vitro qualitative detection of 2019-nCoV antigen from human nasopharyngeal swab, nasal swab or oropharyngeal swab specimens. This kit is suitable for the auxiliary diagnosis of COVID-19, the results are for clinical reference only and cannot be used as the sole basis for diagnosis and exclusion decision. The clinical diagnosis and treatment of patients should be considered in combination with their symptoms/signs, medical history, other laboratory tests and treatment responses. Positive test result needs to be further confirmed, negative result does not preclude 2019-nCoV infection. This kit is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in the techniques of in vitro diagnostic procedures. TEST PRINCIPLE The kit is immunochromatographic and uses double-antibody sandwich method to detect 2019-nCoV N protein antigen. During detection, the treated specimens are loaded into the sample wells of the test card. When the concentration of 2019-nCoV antigen in specimen is higher than the minimum detection limit, the viral antigen will form complexes with labeled antibodies first. Under chromatography, the complexes move forward along the nitrocellulose membrane till captured by pre-coated monoclonal antibody of 2019-nCoV in detection zone on nitrocellulose film (T) to form a pink/purple reaction line on the detection zone, at this point the result is positive; conversely, if there is no viral antigen or the concentration of antigen in specimen is below the minimum detection limit, no pink/purple reaction line appears in the detection zone, at this point the result is negative. Regardless of whether the sample contains viral antigens or not, a pink/purple reaction line will appear in the quality control zone (C), the pink/purple reaction line that appears in the quality control zone (C) is the criterion for determining if the chromatography process is normal.
Self-test received notified body approved CE marking on April 1, 2021 A home test for the rapid qualitative detection of SARS-CoV-2 virus antigen in anterior nasal swabs within 7 days of symptom onset Performance Characteristics Sample type: nasal swab Time to result: 15-20 min Sensitivity: 96.77% Specificity: 99.20% Accuracy: 98.72% Layperson study statistics: o 99.10% of non-professionals carried out the test without requiring assistance o 97.87% of different types of results were interpreted correctly Kit Components: 1 Rapid SARS-CoV-2 Antigen Test Card (sealed foil pouch) 1 sterilized swab 1 extraction tube 1 sample extraction buffer IFU 1 tube stand
