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M-Turbo Mini-Dock

EUDAMED

Class I (EU MDR)

Ref P30375-61Model MINIDOCK DVI, DESKTOP VERSION, M-SERIES

by Fujifilm Sonosite, Inc.

Identity

Trade Name
M-Turbo Mini-Dock EUDAMED
Device Name
MINIDOCK DVI, DESKTOP VERSION, M-SERIES EUDAMED
Model / Reference
MINIDOCK DVI, DESKTOP VERSION, M-SERIES EUDAMED
P30375-61 EUDAMED

Identifiers

Primary DI / UDI-DI
00841517111694 EUDAMED
Basic UDI-DI
B-00841517111694 EUDAMED
EMDN Code
Z1104018099 ULTRASOUND SCANNERS – HARDWARE ACCESSORIES – OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland 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

M-Turbo Mini-Dock by Fujifilm Sonosite, Inc. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

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

Sources (1)

  • EUDAMED b0b72527-6ded-425b-a5dc-0070ab3d2f62 61 fields · synced Jun 18, 2026