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Stellaris BL14304

by Bausch & Lomb Incorporated GUDID 2 variants

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00757770519897 UDI-DIDate24 Sep 2016ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Stellaris
Generic Name
Phacoemulsification/vitrectomy system
Model / Ref / Catalog
BL14304
Primary DI / UDI-DI
00757770519897
FDA Product Code
HQE, HQC
GMDN Term
Phacoemulsification/vitrectomy system
Device Class
Class II
Regulation Number
886.4150, 886.4670
GUDID distribution status
Not in Commercial Distribution

Other devices from Bausch & Lomb Incorporated

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Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No