VS3 Iridium 153-0053
VS3 Iridium 153-0053 is a Class II device made by Visionsense Ltd., listed in FDA GUDID since 7 Aug 2019 (UDI-DI 10813040013858), 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 | Number10813040013858 | Date7 Aug 2019 | StatusListed |
Official records
- AccessGUDID record 10813040013858
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- VS3 Iridium
- Generic name
- Endoscope video camera
- Model / Ref / Catalog
- 153-0053
- Primary DI / UDI-DI
- 10813040013858
- FDA product code
- HRX, GCJ
- GMDN term
- Endoscope video camera
- Device class
- Class II
- Regulation number
- 888.1100, 876.1500
- GUDID distribution status
- In Commercial Distribution
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