Teleflex IPN055295

by Teleflex Incorporated

Teleflex IPN055295 (61114V) is a Class II device made by Teleflex Incorporated, listed in FDA GUDID since 31 Oct 2019 (UDI-DI 24026704666892), 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	Number24026704666892 UDI-DI	Date31 Oct 2019Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 24026704666892

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Teleflex
Generic name: Ligation clip, synthetic polymer, non-bioabsorbable
Model / Ref / Catalog: IPN055295, 61114V

Primary DI / UDI-DI: 24026704666892
FDA product code: FZP
GMDN term: Ligation clip, synthetic polymer, non-bioabsorbable

Device class: Class II
Regulation number: 878.4300
GUDID distribution status: In Commercial Distribution

MRI safety: MR Safe

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Class II

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Properties

Supplied sterile
Single use
Implantable
Prescription use
Lot / batch number
Expiration date

Other properties (9, all answered No)