VS3 114-0002
VS3 114-0002 is a Class I device made by Visionsense Ltd., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 18130400103236), not in commercial distribution (GUDID) as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number18130400103236 | Date23 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 18130400103236
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- VS3
- Generic name
- Endoscope sheath, reusable
- Model / Ref / Catalog
- 114-0002
- Primary DI / UDI-DI
- 18130400103236
- FDA product code
- KAM
- GMDN term
- Endoscope sheath, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- Not in Commercial Distribution
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