Skip to content

Merilas

by Meridian Medical d.o.o.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03830074980048 UDI-DI Date20 Oct 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Ophthalmic solid-state laser system
Model / Ref / Catalog
Merilas 532 alpha, Merilas 532 / 577 / 810 shortpulse, 100491, 100557, 100555, 100580
Primary DI / UDI-DI
03830074980048
FDA Product Code
HQF
GMDN Term
Ophthalmic solid-state laser system
Device Class
Class II
Regulation Number
886.4390
GUDID distribution status
In Commercial Distribution

Other devices from Meridian Medical d.o.o.

Properties

  • Serial Number
  • Manufacturing Date

Other properties (12)

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