Identity
- Trade Name
- HEM-O-LOK APPLIER MEDIUM LARGE 11" RIGHT-ANGLE REFURBISHED EUDAMEDWECK FDA UDI
- Generic Name
- Open-surgery ligation clip applier FDA UDI
- Device Name
- Weck® Hem-o-lok® Ligating Clip Appliers, various Sizes EUDAMEDHEM-O-LOK APPLIER MEDIUM LARGE 11" RIGHT-ANGLE REFURBISHED FDA UDI
- Model / Reference
- 544172R EUDAMEDIPN927245 FDA UDI
- Description
- HEM-O-LOK APPLIER MEDIUM LARGE 11" RIGHT-ANGLE REFURBISHED FDA UDI
Identifiers
- Catalog Number
- 544172R FDA UDI
- Primary DI / UDI-DI
- 14026704760852 EUDAMEDFDA UDI
- Basic UDI-DI
- 08019020000000000000091KM EUDAMED
- Direct Marketing DI
- 24026704760859 EUDAMED
- FDA Product Code
- GDO FDA UDI
- EMDN Code
- L020801 MULTIPLE CLIPS APPLICATORS FOR OPEN SURGERY, REUSABLE EUDAMED
- GMDN Term
- Open-surgery ligation clip applier 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
Yes
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 10.6 Inch FDA UDI
Category: Open-surgery ligation clip applier
Weck by Teleflex Incorporated — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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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 630e7eac-ce07-409f-990c-11559fb84e9e 36 fields · synced Sep 18, 2026
- EUDAMED 1ea50229-b26d-44d9-aaa2-44c3edfc9650 61 fields · synced Sep 18, 2026