Guardian IPN914182

by Teleflex Incorporated

Guardian IPN914182 (8216) is a Class II device made by Teleflex Incorporated, listed in FDA GUDID since 8 Nov 2018 (UDI-DI 10841156101367), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10841156101367 UDI-DI	Date8 Nov 2018Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10841156101367

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Guardian
Generic name: Haemostasis valve
Model / Ref / Catalog: IPN914182, 8216

Primary DI / UDI-DI: 10841156101367
FDA product code: DTL
GMDN term: Haemostasis valve

Device class: Class II
Regulation number: 870.4290
GUDID distribution status: In Commercial Distribution

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Properties

Supplied sterile
Single use
Prescription use
Convenience kit
Lot / batch number
Expiration date

Other properties (9, all answered No)