Visitec® 585176
by Beaver-Visitec International Inc
Visitec® 585176 is a Class I device made by Beaver-Visitec International Inc, listed in FDA GUDID since 3 Dec 2021 (UDI-DI 30886158102060), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number30886158102060 | Date3 Dec 2021 | StatusListed |
Official records
- AccessGUDID record 30886158102060
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Visitec®
- Generic name
- Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use
- Model / Ref / Catalog
- 585176
- Primary DI / UDI-DI
- 30886158102060
- FDA product code
- HMX
- GMDN term
- Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use
- Device class
- Class I
- Regulation number
- 886.4350
- GUDID distribution status
- In Commercial Distribution
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