Weck

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: WECK FDA UDI
Generic Name: Surgical clip remover, reusable FDA UDI
Device Name: HOL PURPLEPLUS L 5MM ENDO REMOVER 35CM FDA UDI
Model / Reference: IPN928702 FDA UDI
Description: HOL PURPLEPLUS L 5MM ENDO REMOVER 35CM FDA UDI

Identifiers

Catalog Number: ME05RVLG FDA UDI
Primary DI / UDI-DI: 14026704921642 FDA UDI
FDA Product Code: GDO FDA UDI
GMDN Term: Surgical clip remover, reusable 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

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Surgical clip remover, reusable

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

Similar devices

Also classified as Surgical clip remover, reusable.

HNM MEDICAL — HNM STAINLESS, LLC. · Class II
Gen2 — SURGIX MEDICAL LLC · Class I
HNM MEDICAL — HNM STAINLESS, LLC. · Class II
MICHEL FORCEPS FOR REMOVING CLIPS — METECH INTERNATIONAL · Class I
HNM MEDICAL — HNM STAINLESS, LLC. · Class II
HNM MEDICAL — HNM STAINLESS, LLC. · Class II
Vitalitec Clip Removers — VITALITEC INTERNATIONAL, INC. · Class I
Vitalitec Clip Removers — VITALITEC INTERNATIONAL, INC. · 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 ed9ad504-5c8f-444a-b7ca-b7c49a6501f4 35 fields · synced Jun 8, 2026