VS3-Ir 519-1825
VS3-Ir 519-1825 is a Class II device made by Visionsense Ltd., listed in FDA GUDID since 1 Apr 2021 (UDI-DI 10884521810181), registry data 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 | Number10884521810181 | Date1 Apr 2021 | StatusListed |
Official records
- AccessGUDID record 10884521810181
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- VS3-Ir
- Generic name
- Endoscope video camera
- Model / Ref / Catalog
- 519-1825
- Primary DI / UDI-DI
- 10884521810181
- FDA product code
- OWN
- GMDN term
- Endoscope video camera
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
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