Ground Stock is available in Istanbul Bonded warehouse
Procedure:
1.Buyer sends their interntion via Loi
2.Seller sends Proforma Invoice
3.Buyer sends Proof of Funds
4.Buyer makes a visit to the warehouse to check the stock
5.Both parties sign SPA, Sales Purchase agreement
6.Funds transfer, and products own by buyer
Disposable gloves
Color:Blue
100% Nitrile, powder-free, non-sterile.
Long cuffs (at least 230 mm total length)
Sizes: S,M,L, XL
Norms / standards:
- Directive 93/42 / EEC Category III
- Regulation (EU) 2016/425 category III
- EN 455 (1&2)
- EN 374
- ANSI / ISEA 105
- ASTM D6319 or equivalent standards
Test results and certifications are available
Manufactured by latest version of German Weber machines
The requirements and standarts apply to equipment intended for use in
Residential (domestic) environment
Commercial and light industrial environment
Industrial Environment
Medical Environment
per annum. Price for volume over the MoQ 30 Million boxes is negotiable. Payment by L/C 100% at sight, transferable, irrevocable and confirmed.
Product Name: Disposable Vinyl/Nitrile Blended Examination Gloves
Single use, non-sterile, no measuring, Latex free
Sizes: XS, M, L. XL. XXL
Color: Blue, Green
Structure: 5 fingers, beaded cuff for easy donning, ambidextrous
Surface: Smooth
The Vinyl/Nitrile Blended glove is a new type of synthetic glove that was
developed based on the vinyl glove production technology. Its material is
compounded with PVC paste and Nitrile latex, so the finished production has
the advantage of both PVC and Nitrile gloves.
Comparing with the vinyl gloves, the Vinyl/Nitrile Blended glove can better
satisfy the users demands, it feels softer, more flexible and more
comfortable when wearing.
Intended purpose: The examination glove is disposable non-sterile device
intended for medical purpose that is worn on the examinerâ??s hand or finger
to prevent contamination between patient and examiner.
Medical Device Quality Management System EN ISO 13485 Certificate,
ISO 9001 Quality Management System Certificate - 2 FDA
FDA Registration Information - 510K
Product 510K
Biocompatibility Test Report
EU CE Certificate (DOC, Technical Documentation Review Report
)
