Bausch + Lomb CX6802
Bausch + Lomb CX6802 is a vitrectomy system micro-cutting unit (FDA Class II; FDA product code HQE, Instrument, Vitreous Aspiration And Cutting, Ac-Powered) made by Bausch & Lomb Incorporated, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 20757770482614), 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 | Number20757770482614 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 20757770482614
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Bausch + Lomb
- Generic name
- Vitrectomy system micro-cutting unit
- Model / Ref / Catalog
- CX6802
- Primary DI / UDI-DI
- 20757770482614
- FDA product code
- HQE
- GMDN term
- Vitrectomy system micro-cutting unit
- Device class
- Class II
- Regulation number
- 886.4150
- GUDID distribution status
- In Commercial Distribution
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