BluTouch TNR 700S
BluTouch TNR 700S is a Class I device made by Mercedes Medical LLC, cleared under FDA 510(k) K110981 and listed in FDA GUDID since 28 Dec 2022 (UDI-DI 00860008185105), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00860008185105 | Date28 Dec 2022 | StatusListed |
| United States | FDA 510(k) | NumberK110981 | Date— | StatusActive |
Official records
- AccessGUDID record 00860008185105
- FDA 510(k) database K110981
Across registries
- FDA 510(k) K110981 Active
- FDA GUDID UDI-DI 00860008185105 listed 28 Dec 2022 Listed
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- BluTouch
- Generic name
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial
- Model / Ref / Catalog
- TNR 700S
- Primary DI / UDI-DI
- 00860008185105
- 510(k) Number
- FDA product code
- LZA
- GMDN term
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial
- Device class
- Class I
- Regulation number
- 880.6250
- GUDID distribution status
- In Commercial Distribution
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