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Peak Medical 33-16901

by PEAK MEDICAL Distribution Inc

Peak Medical 33-16901 is a Class I device made by PEAK MEDICAL Distribution Inc, listed in FDA GUDID since 19 Jun 2026 (UDI-DI G45333169010), 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 NumberG45333169010 UDI-DI Date19 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  • Withdrawn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
Endaural surgical curette, reusable
Model / reference
33-16901
Primary DI / UDI-DI
G45333169010
FDA product code
KTG
GMDN term
Endaural surgical curette, reusable
Device class
Class I
Regulation number
874.4420
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)