Identity
- Trade Name
- Jaco® EUDAMED
- Device Name
- Jaco® EUDAMED
- Model / Reference
- AO 0000 0001 EUDAMEDKR MJ2 0001 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 62867894100021 EUDAMED62867894100014 EUDAMED
- Basic UDI-DI
- 628678941PJ00900006B5 EUDAMED
- Direct Marketing DI
- 62867894100014 EUDAMED
- EMDN Code
- Y242199 DEVICES FOR REACHING AND GRASPING OBJECTS - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany 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
Jaco® by Kinova — 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 | 628678941PJ00900006B5 | Class I | Active |
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Manufacturer
- Manufacturer
- Kinova
- EUDAMED SRN
- CA-MF-000003231
- Authorised Representative
- AR Experts B.V. NL-AR-000023989
Sources (2)
- EUDAMED bdd73323-3972-4137-bf13-c47799412682 61 fields · synced Jul 10, 2026
- EUDAMED f89d9bf3-e7dc-4c60-8fe5-c914b7c278b9 61 fields · synced May 16, 2026