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M-Turbo Mini-Dock
EUDAMEDFDA UDIClass I (EU MDR)
Ref P30375-01Model MINIDOCK DVI, DESKTOP VERSION, M-SERIES
Identity
- Trade Name
- M-Turbo Mini-Dock EUDAMEDFDA UDI
- Generic Name
- Noninvasive device battery charger FDA UDI
- Device Name
- MINIDOCK DVI, DESKTOP VERSION, M-SERIES EUDAMEDDiagnostic Ultrasound Transducer FDA UDI
- Model / Reference
- MINIDOCK DVI, DESKTOP VERSION, M-SERIES EUDAMEDP30375-01 EUDAMEDFDA UDI
- Description
- Diagnostic Ultrasound Transducer FDA UDI
Identifiers
- Catalog Number
- P30375 FDA UDI
- Primary DI / UDI-DI
- 00841517108106 EUDAMEDFDA UDI
- Basic UDI-DI
- 08415171MNDCKFP EUDAMED
- 510(k) Number
- K130173 FDA UDI
- FDA Product Code
- IYN FDA UDIIYO FDA UDIOIJ FDA UDIITX FDA UDI
- EMDN Code
- Z1104018099 ULTRASOUND SCANNERS – HARDWARE ACCESSORIES – OTHER EUDAMED
- GMDN Term
- Noninvasive device battery charger FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 892.1550 FDA UDI892.1560 FDA UDI892.1570 FDA UDI
- 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
M-Turbo Mini-Dock 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 | 08415171MNDCKFP | 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 7ec84022-50f5-4ab7-9eed-eef0b5625e4a 61 fields · synced Jul 18, 2026
- FDA UDI 091fb06c-f008-4831-b149-7d1c269a17d4 36 fields · synced May 30, 2026