Identity
- Trade Name
- HYBRIDknife® flex T-Type EUDAMED
- Device Name
- HYBRIDknife® flex EUDAMED
- Model / Reference
- 20150-110 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04050147022942 EUDAMED
- Basic UDI-DI
- 4050147HYBRIDknifeflex-GS EUDAMED
- Direct Marketing DI
- 04050147022942 EUDAMED
- EMDN Code
- K0201010301 OPEN ELECTROSURGERY ELECTRODES, SINGLE-USE EUDAMED
Classification
- Device Class
- Class IIb EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
Yes
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
Yes
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Category: Open-surgery electrosurgical electrode, monopolar, single-use
HYBRIDknife® flex T-Type by Erbe Elektromedizin GmbH — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS
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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 | 4050147HYBRIDknifeflex-GS | Class IIb | Active |
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Manufacturer
- Manufacturer
- Erbe Elektromedizin GmbH
- EUDAMED SRN
- DE-MF-000005498
Sources (1)
- EUDAMED 490a887a-762c-427f-8750-1fadd0fd3956 61 fields · synced Sep 19, 2026