Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: PILLING FDA UDI
Generic Name: Gynaecological cerclage needle FDA UDI
Device Name: NEEDLE GUIDE IOWA TRMPT SHAPE STR 5-1/2" FDA UDI
Model / Reference: IPN017875 FDA UDI
Description: NEEDLE GUIDE IOWA TRMPT SHAPE STR 5-1/2" FDA UDI

Identifiers

Catalog Number: P16288 FDA UDI
Primary DI / UDI-DI: 14026704792099 FDA UDI
FDA Product Code: KOA FDA UDI
GMDN Term: Gynaecological cerclage needle FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 876.4730 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: Gynaecological cerclage needle

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

Similar devices

Also classified as Gynaecological cerclage needle.

Greenwald Surgical Company, Inc. — GRACE MANUFACTURING INC · Class II
Greenwald Surgical Company, Inc. — GRACE MANUFACTURING INC · Class II
PILLING — TELEFLEX INCORPORATED · Class I

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 3d252781-9079-4e7c-b6b8-747968e746ed 35 fields · synced May 30, 2026