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Bausch + Lomb CX6805

by Bausch & Lomb Incorporated

Bausch + Lomb CX6805 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 20757770482621), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number20757770482621 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Bausch + Lomb
Generic name
Vitrectomy system micro-cutting unit
Model / Ref / Catalog
CX6805
Primary DI / UDI-DI
20757770482621
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

Similar devices

Other devices filed under FDA product code HQE (Instrument, Vitreous Aspiration And Cutting, Ac-Powered).

Other devices from Bausch & Lomb Incorporated

See all devices from Bausch & Lomb Incorporated →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)