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Battery
EUDAMEDFDA UDIClass I (EU MDR)
Ref P15051-25Model BATTERY PACK ASSEMBLY, 6 CELL, LITHIUM-ION, EDGE
Identity
- Trade Name
- Battery EUDAMEDFDA UDI
- Generic Name
- Portable/mobile rechargeable battery pack FDA UDI
- Device Name
- BATTERY PACK ASSEMBLY, 6 CELL, LITHIUM-ION, EDGE EUDAMEDDiagnostic Ultrasound System Accessory. Battery mounted internally within an ultrasound system. FDA UDI
- Model / Reference
- BATTERY PACK ASSEMBLY, 6 CELL, LITHIUM-ION, EDGE EUDAMEDP15051-25 EUDAMEDFDA UDI
- Description
- Diagnostic Ultrasound System Accessory. Battery mounted internally within an ultrasound system. FDA UDI
Identifiers
- Catalog Number
- P15051 FDA UDI
- Primary DI / UDI-DI
- 00841517105983 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00841517105983 EUDAMED
- 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
- 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 — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00841517105983 | 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 176f176b-d026-4a86-ba7c-a6576f605e72 61 fields · synced Jul 21, 2026
- FDA UDI ef1f2510-f0fa-494f-8659-ad4c12a2acb9 36 fields · synced May 30, 2026