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Rusch IPN924559

by Teleflex Incorporated

Rusch IPN924559 (1140) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 4 Apr 2023 (UDI-DI 14026704743718), 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 Number14026704743718 UDI-DI Date4 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  • Withdrawn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
Rusch
Generic name
Endoscopic bite block, basic, single-use
Model / Ref / Catalog
IPN924559, 1140
Primary DI / UDI-DI
14026704743718
FDA product code
MNK
GMDN term
Endoscopic bite block, basic, single-use
Device class
Class I
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic bite block, basic, single-use

Similar devices in this category

Other devices filed under Endoscopic bite block, basic, single-use.

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See all devices from Teleflex Incorporated →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)