Identity
- Trade Name
- OCTOPUS EUDAMED
- Device Name
- OCTOPUS EUDAMED
- Model / Reference
- H007 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03770019196052 EUDAMED
- Basic UDI-DI
- 3770019196H007TF EUDAMED
- Direct Marketing DI
- 03770019196052 EUDAMED
- EMDN Code
- Z1205078099 INSTRUMENTS FOR CARDIOLOGICAL POLYGRAPHY - HARDWARE ACCESSORIES - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- France 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
Octopus by Substrate Hd — 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 | 3770019196H007TF | Class I | Active |
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Manufacturer
- Manufacturer
- Substrate HD
- EUDAMED SRN
- FR-MF-000000507
Sources (1)
- EUDAMED aedb8fbb-097d-4eb0-a091-62d1f0bb65e3 61 fields · synced Jun 18, 2026