Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: PILLING FDA UDI
Generic Name: Surgical bulldog clamp, reusable FDA UDI
Device Name: LARGE VESSEL CLIP 24MM TAPERED BLADES FDA UDI
Model / Reference: IPN002320 FDA UDI
Description: LARGE VESSEL CLIP 24MM TAPERED BLADES FDA UDI

Identifiers

Catalog Number: 065111 FDA UDI
Primary DI / UDI-DI: 24026704506952 FDA UDI
510(k) Number: K861924 FDA UDI
FDA Product Code: DXC FDA UDI
GMDN Term: Surgical bulldog clamp, 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 — 1.61 Inch FDA UDI
Width — 0.203 Inch FDA UDI

Category: Surgical bulldog clamp, reusable

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

Similar devices

Also classified as Surgical bulldog clamp, reusable.

V. Mueller — STERIS CORPORATION · Class II
ATRAUMATA — AESCULAP, INC. · Class I
Integra® Jarit® — Integra LifeSciences Production Corporation · Class II
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
Avalign — AVALIGN TECHNOLOGIES, Inc. · Class II
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
Symmetry Surgical — SYMMETRY SURGICAL INC. · Class II
AESCULAP — AESCULAP, INC. · Class II

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI 9781d112-352e-455f-8daa-2ee13ae19e03 37 fields · synced Jun 6, 2026