Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: PILLING FDA UDI
Generic Name: Wire/ligature passer, reusable FDA UDI
Device Name: FAVA-SEMB Ligature Carrier HALF Curved Autragrip FDA UDI
Model / Reference: IPN005757 FDA UDI
Description: FAVA-SEMB Ligature Carrier HALF Curved Autragrip FDA UDI

Identifiers

Catalog Number: 353645 FDA UDI
Primary DI / UDI-DI: 24026704520460 FDA UDI
510(k) Number: K861924 FDA UDI
FDA Product Code: DXC FDA UDI
GMDN Term: Wire/ligature passer, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.4450 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

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 — 28.5 Centimeter FDA UDI

Category: Wire/ligature passer, reusable

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

Similar devices

Also classified as Wire/ligature passer, reusable.

Novo Surgical — NOVO SURGICAL, INC. · Class I
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I
Marina Medical — MARINA MEDICAL INSTRUMENTS, INC. · Class I
V. Mueller — STERIS CORPORATION · Class I
Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I

Cleared under the same submission

K861924 also covers:

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 10b0d9f3-5d36-404d-8b2d-e1d24bffeaa2 37 fields · synced Jun 1, 2026