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Peak Medical 33-0629

by PEAK MEDICAL Distribution Inc

Peak Medical 33-0629 is a Class I device made by PEAK MEDICAL Distribution Inc, listed in FDA GUDID since 24 Jun 2026 (UDI-DI G4533306290), 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 NumberG4533306290 UDI-DI Date24 Jun 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Peak Medical
Generic name
Ophthalmic surgical probe, reusable
Model / reference
33-0629
Primary DI / UDI-DI
G4533306290
FDA product code
HND
GMDN term
Ophthalmic surgical probe, reusable
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from PEAK MEDICAL Distribution Inc

See all devices from PEAK MEDICAL Distribution Inc →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)