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Power Park
EUDAMEDClass I (EU MDR)
Ref P31109-01Model ASSEMBLY, POWERPARK DOCK MODULE
Identity
- Trade Name
- Power Park EUDAMED
- Device Name
- ASSEMBLY, POWERPARK DOCK MODULE EUDAMED
- Model / Reference
- ASSEMBLY, POWERPARK DOCK MODULE EUDAMEDP31109-01 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00841517108298 EUDAMED
- Basic UDI-DI
- 08415171PWRPRKDCKMDLFD EUDAMED
- EMDN Code
- Z1104018099 ULTRASOUND SCANNERS – HARDWARE ACCESSORIES – OTHER EUDAMED
Classification
- Device Class
- Class I 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
Power Park by Fujifilm Sonosite, Inc. — 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 | 08415171PWRPRKDCKMDLFD | Class I | Active |
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Manufacturer
- Manufacturer
- Fujifilm Sonosite, Inc.
- EUDAMED SRN
- US-MF-000001075
- Authorised Representative
- Fujifilm Sonosite B.V. NL-AR-000000046
Sources (1)
- EUDAMED a51de072-e72a-49ee-ae83-f44bd6e154fe 61 fields · synced Jun 18, 2026