Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: PILLING FDA UDI
Generic Name: Uterine tenaculum FDA UDI
Device Name: M.G.H. FORCEPS 3X3 TEETH, 6", 15.24CM FDA UDI
Model / Reference: IPN004498 FDA UDI
Description: M.G.H. FORCEPS 3X3 TEETH, 6", 15.24CM FDA UDI

Identifiers

Catalog Number: 213175 FDA UDI
Primary DI / UDI-DI: 24026704514902 FDA UDI
FDA Product Code: HTD FDA UDI
GMDN Term: Uterine tenaculum FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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 — 156 Millimeter FDA UDI

Category: Uterine tenaculum

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

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Integra® Miltex® — Integra LifeSciences Production Corporation · Class II
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 I	Pending data

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Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI 2154eda3-6ddd-4ca4-9d1b-ec276740d938 36 fields · synced May 30, 2026