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Bausch + Lomb E3096L 9.50

by Bausch & Lomb Incorporated

Bausch + Lomb E3096L 9.50 is a Class I device made by Bausch & Lomb Incorporated, listed in FDA GUDID since 25 Sep 2016 (UDI-DI 10757770055804), 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 Number10757770055804 UDI-DI Date25 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  • Withdrawn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
Corneal trephine, single-use
Model / Ref / Catalog
E3096L 9.50
Primary DI / UDI-DI
10757770055804
FDA product code
HRH
GMDN term
Corneal trephine, single-use
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Corneal trephine, single-use

Similar devices in this category

Other devices filed under Corneal trephine, single-use.

Other devices from Bausch & Lomb Incorporated

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Properties

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