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Power Park
EUDAMEDFDA UDIClass I (EU MDR)
Ref P25003-17Model ASSEMBLY, POWERPARK DOCK MODULE
Identity
- Trade Name
- Power Park EUDAMEDFDA UDI
- Generic Name
- Electromechanical device/system transport trolley FDA UDI
- Device Name
- ASSEMBLY, POWERPARK DOCK MODULE EUDAMEDDiagnostic ultrasound system FDA UDI
- Model / Reference
- ASSEMBLY, POWERPARK DOCK MODULE EUDAMEDP25003-17 EUDAMEDFDA UDI
- Description
- Diagnostic ultrasound system FDA UDI
Identifiers
- Catalog Number
- P25003 FDA UDI
- Primary DI / UDI-DI
- 00841517109738 EUDAMEDFDA UDI
- Basic UDI-DI
- 08415171PWRPRKDCKMDLFD EUDAMED
- FDA Product Code
- ITX FDA UDIIYO FDA UDIIYN FDA UDI
- EMDN Code
- Z1104018099 ULTRASOUND SCANNERS – HARDWARE ACCESSORIES – OTHER EUDAMED
- GMDN Term
- Electromechanical device/system transport trolley FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 892.1570 FDA UDI892.1560 FDA UDI892.1550 FDA UDI
- Market of Registration
- Austria EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
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
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Power Park by Fujifilm Sonosite, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 08415171PWRPRKDCKMDLFD | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Fujifilm Sonosite, Inc.
- EUDAMED SRN
- US-MF-000001075
- Authorised Representative
- Fujifilm Sonosite B.V. NL-AR-000000046
Sources (2)
- EUDAMED 52138a3e-d494-4372-a831-0640f31c618c 61 fields · synced Jun 18, 2026
- FDA UDI b458547c-273b-4afb-b9e6-af3a18170242 36 fields · synced May 30, 2026