Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: PILLING FDA UDI
Generic Name: Uterine tenaculum FDA UDI
Device Name: FORCEPS HEANEY HEAVY SINGLE GROOVED 8 7/16" FDA UDI
Model / Reference: IPN004517 FDA UDI
Description: FORCEPS HEANEY HEAVY SINGLE GROOVED 8 7/16" FDA UDI

Identifiers

Catalog Number: 214172 FDA UDI
Primary DI / UDI-DI: 24026704514971 FDA UDI
FDA Product Code: KNA FDA UDI
GMDN Term: Uterine tenaculum FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.4530 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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Unsafe FDA UDI

Dimensions & Sizes

Size: Length — 21 Centimeter FDA UDI

Category: Uterine tenaculum

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

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Also classified as Uterine tenaculum.

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GEN2 — SURGIX MEDICAL LLC · Class II
GEN2 — SURGIX MEDICAL LLC · Class II

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 369ec14c-4842-4018-96af-ae4fde947b92 36 fields · synced Jun 6, 2026