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Olympus TC-E300

by KeyMed (Medical and Industrial Equipment) Ltd

Olympus TC-E300 is a Class I device made by KeyMed (Medical and Industrial Equipment) Ltd, listed in FDA GUDID since 24 Sep 2019 (UDI-DI 15019778005218), 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 Number15019778005218 UDI-DI Date24 Sep 2019ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Olympus
Generic name
Surgical suction pump
Model / reference
TC-E300
Primary DI / UDI-DI
15019778005218
FDA product code
FEM
GMDN term
Surgical suction pump
Device class
Class I
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical suction pump

Similar devices

Also classified as Surgical suction pump.

Other devices from KeyMed (Medical and Industrial Equipment) Ltd

See all devices from KeyMed (Medical and Industrial Equipment) Ltd →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)