Skip to content

Bausch + Lomb DP5100

by Bausch & Lomb Incorporated

Bausch + Lomb DP5100 is a vitrectomy fluid/gas handling handpiece/cannula (FDA Class II; FDA product code HQC, Unit, Phacofragmentation) made by Bausch & Lomb Incorporated, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10757770055255), 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 Number10757770055255 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  • Withdrawn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 fluid/gas handling handpiece/cannula
Model / Ref / Catalog
DP5100
Primary DI / UDI-DI
10757770055255
FDA product code
HQC
GMDN term
Vitrectomy fluid/gas handling handpiece/cannula
Device class
Class II
Regulation number
886.4670
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vitrectomy fluid/gas handling handpiece/cannula

Similar devices in this category

Other devices filed under Vitrectomy fluid/gas handling handpiece/cannula.

Other devices from Bausch & Lomb Incorporated

See all devices from Bausch & Lomb Incorporated →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)