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: IOWA TRUMPET NEEDLE GUIDE FDA UDI
Model / Reference: IPN010253 FDA UDI
Description: IOWA TRUMPET NEEDLE GUIDE FDA UDI

Identifiers

Catalog Number: 884227 FDA UDI
Primary DI / UDI-DI: 24026704204506 FDA UDI
FDA Product Code: HTD FDA UDI
GMDN Term: Gynaecological cerclage needle 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

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 140 Millimeter FDA UDI
Width — 45 Millimeter 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 825a7db9-1058-48bb-8909-f74f08936848 36 fields · synced May 31, 2026