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Mouthpiece MB-142

by Olympus Medical Systems Corporation

Mouthpiece MB-142 (N6178401) is a Class I device made by Olympus Medical Systems Corporation, listed in FDA GUDID since 22 Apr 2023 (UDI-DI 04953170438257), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04953170438257 UDI-DI Date22 Apr 2023ListedStatusListed 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  • Withdrawn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
Mouthpiece
Generic name
Endoscopic bite block, basic, reusable
Model / Ref / Catalog
MB-142, N6178401
Primary DI / UDI-DI
04953170438257
FDA product code
MNK
GMDN term
Endoscopic bite block, basic, reusable
Device class
Class I
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic bite block, basic, reusable

Other devices from Olympus Medical Systems Corporation

See all devices from Olympus Medical Systems Corporation →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)