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Defibrillation Electrode
EUDAMEDClass I (EU MDR)
Ref GC-DF032Model GC-DF019 GC-DF020 GC-DF021 GC-DF022 GC-DF023 GC-DF024 GC-DF025 GC-DF026 GC-DF027 GC-DF028 GC-DF029 GC-DF030 GC-DF031 GC-DF032 GC-DF033 GC-DF034 GC-DF035 GC-DF036 GC-DF037 etc
Identity
- Device Name
- Defibrillation Electrode EUDAMED
- Model / Reference
- GC-DF019 GC-DF020 GC-DF021 GC-DF022 GC-DF023 GC-DF024 GC-DF025 GC-DF026 GC-DF027 GC-DF028 GC-DF029 GC-DF030 GC-DF031 GC-DF032 GC-DF033 GC-DF034 GC-DF035 GC-DF036 GC-DF037 etc EUDAMEDGC-DF032 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06977563443138 EUDAMED
- Basic UDI-DI
- 697756344Defibrillation4K EUDAMED
- EMDN Code
- Z12030585 DEFIBRILLATORS - CONSUMABLES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Austria EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
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
Defibrillation Electrode by Dongguan Goceng Medical Supplies Co., Ltd — 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 | 697756344Defibrillation4K | Class I | Active |
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Manufacturer
- Manufacturer
- Dongguan Goceng Medical Supplies Co., Ltd
- EUDAMED SRN
- CN-MF-000042512
- Authorised Representative
- SUNGO Europe B.V. NL-AR-000000247
Sources (1)
- EUDAMED f5c61930-470b-486a-9356-c58014962f53 61 fields · synced Jun 20, 2026