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Battery
EUDAMEDFDA UDIClass I (EU MDR)
Ref P30205-02Model KIT, BATTERY AND ACCESSORY, SONOSITE LX
Identity
- Trade Name
- Battery EUDAMEDFDA UDI
- Generic Name
- Portable/mobile rechargeable battery pack FDA UDI
- Device Name
- KIT, BATTERY AND ACCESSORY, SONOSITE LX EUDAMEDDiagnostic Ultrasound System Accessory. Battery mounted internally within an ultrasound system FDA UDI
- Model / Reference
- KIT, BATTERY AND ACCESSORY, SONOSITE LX EUDAMEDP30205-02 EUDAMEDFDA UDI
- Description
- Diagnostic Ultrasound System Accessory. Battery mounted internally within an ultrasound system FDA UDI
Identifiers
- Catalog Number
- P30205 FDA UDI
- Primary DI / UDI-DI
- 00841517110246 EUDAMEDFDA UDI
- Basic UDI-DI
- 08415171BATACC7T EUDAMED
- 510(k) Number
- K233597 FDA UDI
- FDA Product Code
- ITX FDA UDIIYN FDA UDIIYO FDA UDI
- EMDN Code
- Z1104018099 ULTRASOUND SCANNERS – HARDWARE ACCESSORIES – OTHER EUDAMED
- GMDN Term
- Portable/mobile rechargeable battery pack FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 892.1570 FDA UDI892.1550 FDA UDI892.1560 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
Battery 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 | 08415171BATACC7T | 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 52d2744b-b971-42c3-bc9d-871926c15103 61 fields · synced May 31, 2026
- FDA UDI 7eead484-87df-4534-b632-f3d15f380539 36 fields · synced May 29, 2026