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Peak Medical 33-1096

by PEAK MEDICAL Distribution Inc

Peak Medical 33-1096 is a Class I device made by PEAK MEDICAL Distribution Inc, listed in FDA GUDID since 19 Oct 2026 (UDI-DI G4533310960), registry data as of 2 Nov 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 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberG4533310960 UDI-DI Date19 Oct 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  • Withdrawn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
Surgical retractor/retraction system blade, reusable
Model / reference
33-1096
Primary DI / UDI-DI
G4533310960
FDA product code
GAD
GMDN term
Surgical retractor/retraction system blade, reusable
Device class
Class I
Regulation number
878.4800
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)