Weck

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: WECK FDA UDI
Generic Name: Ligation clip, metallic FDA UDI
Device Name: HEMOCLIP TA MED 25 Clips/Cart FDA UDI
Model / Reference: IPN008502 FDA UDI
Description: HEMOCLIP TA MED 25 Clips/Cart FDA UDI

Identifiers

Catalog Number: 523101 FDA UDI
Primary DI / UDI-DI: 34026704600503 FDA UDI
510(k) Number: K132658 FDA UDI
FDA Product Code: FZP FDA UDI
GMDN Term: Ligation clip, metallic FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4300 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Height — 4.49 Millimeter FDA UDI
Length — 5.79 Millimeter FDA UDI

Category: Ligation clip, metallic

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

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SLS-CLIP VITALITEC — PETERS SURGICAL · Class II

Cleared under the same submission

K132658 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 15c0930a-dd33-46f4-b6c5-4c71850150e7 37 fields · synced May 31, 2026