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Guardian IPN914196

by Teleflex Incorporated

Guardian IPN914196 (FH101-T) is a Class II device made by Teleflex Incorporated, listed in FDA GUDID since 8 Nov 2018 (UDI-DI 10841156101954), 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 Number10841156101954 UDI-DI Date8 Nov 2018ListedStatusListed 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  • Withdrawn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
Guardian
Generic name
Haemostasis valve
Model / Ref / Catalog
IPN914196, FH101-T
Primary DI / UDI-DI
10841156101954
FDA product code
DTL
GMDN term
Haemostasis valve
Device class
Class II
Regulation number
870.4290
GUDID distribution status
In Commercial Distribution

Related devices

Category: Haemostasis valve

Similar devices in this category

Other devices filed under Haemostasis valve.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)