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Peak Medical 33-12BT

by PEAK MEDICAL Distribution Inc

Peak Medical 33-12BT is a Class I device made by PEAK MEDICAL Distribution Inc, listed in FDA GUDID since 3 Jun 2026 (UDI-DI G4533312BT0), 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 NumberG4533312BT0 UDI-DI Date3 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  • Withdrawn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
Surgical/emergency suction cannula, non-illuminating, reusable
Model / reference
33-12BT
Primary DI / UDI-DI
G4533312BT0
FDA product code
LXH
GMDN term
Surgical/emergency suction cannula, non-illuminating, reusable
Device class
Class I
Regulation number
888.4540
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)