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HEISS Arterienklemme
EUDAMEDClass I (EU MDR)
Ref 12-3900-20Model Klemme, Arterie
Identity
- Trade Name
- HEISS Arterienklemme EUDAMED
- Model / Reference
- Klemme, Arterie EUDAMED12-3900-20 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250379817013 EUDAMED
- Basic UDI-DI
- 4250485300000016Z4 EUDAMED
- Direct Marketing DI
- 04250379817013 EUDAMED
- EMDN Code
- L07080102 GENERIC VASCULAR CLAMPING ANGIOSTATS AND FORCEPS, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMED
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
HEISS Arterienklemme by Zepf Medical Instruments GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 4250485300000016Z4 | Class I | Active |
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Manufacturer
- Manufacturer
- Zepf Medical Instruments GmbH
- EUDAMED SRN
- DE-MF-000005528
Sources (1)
- EUDAMED d8280ab1-e161-4ad6-bb19-8a100523324c 61 fields · synced Aug 1, 2026