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: Kleinert-Kutz MICRO CLIP Curved 6MM X 1MM BLADES FDA UDI
Model / Reference: IPN002322 FDA UDI
Description: Kleinert-Kutz MICRO CLIP Curved 6MM X 1MM BLADES FDA UDI

Identifiers

Catalog Number: 065145 FDA UDI
Primary DI / UDI-DI: 24026704506976 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

Yes

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 — 0.47 Inch FDA UDI
Width — 0.17 Inch FDA UDI

Category: Surgical bulldog clamp, reusable

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

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Also classified as Surgical bulldog clamp, reusable.

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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

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Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI 49b0aeaf-f529-4be7-88f7-3e2582e2e6b5 37 fields · synced Jun 1, 2026