Identity
- Trade Name
- HEM-O-LOK OPEN REMOVER MEDIUM/MEDIUM-LARGE/LARGE 11" EUDAMEDWECK FDA UDI
- Generic Name
- Surgical clip remover, reusable FDA UDI
- Device Name
- Weck® Hem-o-lok® Ligating Clip Removers, various s EUDAMEDHEM-O-LOK OPEN REMOVER MEDIUM/MEDIUM-LARGE/LARGE 11" FDA UDI
- Model / Reference
- 544123 EUDAMEDIPN921531 FDA UDI
- Description
- HEM-O-LOK OPEN REMOVER MEDIUM/MEDIUM-LARGE/LARGE 11" FDA UDI
Identifiers
- Catalog Number
- 544123 FDA UDI
- Primary DI / UDI-DI
- 14026704727329 EUDAMEDFDA UDI
- Basic UDI-DI
- 08019020000000000000008K8 EUDAMED
- Direct Marketing DI
- 44026704727320 EUDAMED
- FDA Product Code
- GDO FDA UDI
- EMDN Code
- L21 CLIP REMOVAL SURGICAL FORCEPS, REUSABLE EUDAMED
- GMDN Term
- Surgical clip remover, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 10.5 Inch FDA UDI
Category: Surgical clip remover, reusable
Weck by Teleflex Incorporated — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — 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 (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (2)
- FDA UDI 111b91dd-78b7-48c4-8112-e668845a1490 36 fields · synced Jun 18, 2026
- EUDAMED 8bb27e38-5f30-4813-9d99-28ba6bd79aad 61 fields · synced Jun 18, 2026