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Taut IPN006592

by Teleflex Incorporated

Taut IPN006592 (4050788S) is a Class II device made by Teleflex Incorporated, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 24026704505177), 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 Number24026704505177 UDI-DI Date16 Sep 2016ListedStatusListed 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  • Withdrawn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
Taut
Generic name
Rigid endoscope obturator
Model / Ref / Catalog
IPN006592, 4050788S
Primary DI / UDI-DI
24026704505177
FDA product code
GCJ
GMDN term
Rigid endoscope obturator
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 70 Millimeter

Related devices

Category: Rigid endoscope obturator

Similar devices in this category

Other devices filed under Rigid endoscope obturator.

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)