Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: PILLING FDA UDI
Generic Name: Open-surgery ligation clip applier FDA UDI
Device Name: CLAMP SINGLE HAND APPLD BLACK 2.0-5MM FDA UDI
Model / Reference: IPN018816 FDA UDI
Description: CLAMP SINGLE HAND APPLD BLACK 2.0-5MM FDA UDI

Identifiers

Catalog Number: P18658 FDA UDI
Primary DI / UDI-DI: 14026704652553 FDA UDI
FDA Product Code: FHN FDA UDI
GMDN Term: Open-surgery ligation clip applier FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.4400 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Open-surgery ligation clip applier

Pilling by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI abcac3c8-5b28-4432-9697-85a612c523e8 35 fields · synced May 30, 2026