ViaMed 17001-R
ViaMed 17001-R is a Class II device made by Rece International Corp., cleared under FDA 510(k) K082042 on 3 Sep 2008 and listed in FDA GUDID since 20 May 2019 (UDI-DI 00811382013119), 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 | Number00811382013119 | Date20 May 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK082042 | Date3 Sep 2008 | StatusActive |
Official records
- AccessGUDID record 00811382013119
- FDA 510(k) database K082042
Across registries
- FDA 510(k) K082042 decided 3 Sep 2008 Active
- FDA GUDID UDI-DI 00811382013119 listed 20 May 2019 Listed
Timeline
- Cleared FDA 510(k) K082042
- Listed FDA GUDID 00811382013119
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- ViaMed
- Generic name
- Contaminated waste container
- Model / reference
- 17001-R
- Primary DI / UDI-DI
- 00811382013119
- 510(k) Number
- FDA product code
- MMK
- GMDN term
- Contaminated waste container
- Device class
- Class II
- Regulation number
- 880.5570
- GUDID distribution status
- In Commercial Distribution
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