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Battery

EUDAMED

Class I (EU MDR)

Ref P31068-01Model KIT, BATTERY AND ACCESSORY, SONOSITE LX

by Fujifilm Sonosite, Inc.

Identity

Trade Name
Battery EUDAMED
Device Name
KIT, BATTERY AND ACCESSORY, SONOSITE LX EUDAMED
Model / Reference
KIT, BATTERY AND ACCESSORY, SONOSITE LX EUDAMED
P31068-01 EUDAMED

Identifiers

Primary DI / UDI-DI
00841517107741 EUDAMED
Basic UDI-DI
08415171BATACC7T 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

Battery 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

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Manufacturer

EUDAMED SRN
US-MF-000001075
Authorised Representative
Fujifilm Sonosite B.V. NL-AR-000000046

Sources (1)

  • EUDAMED 1dbb5bbd-31d6-4b62-8dfe-ac701dc9225b 61 fields · synced May 22, 2026