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L13-6

EUDAMED

Class IIa (EU MDR)

Ref P32614-02Model TRANSDUCER, L13-6

by Fujifilm Sonosite, Inc.

Identity

Trade Name
L13-6 EUDAMED
Device Name
TRANSDUCER, L13-6 EUDAMED
Model / Reference
TRANSDUCER, L13-6 EUDAMED
P32614-02 EUDAMED

Identifiers

Primary DI / UDI-DI
00841517111243 EUDAMED
Basic UDI-DI
08415171L136BU EUDAMED
EMDN Code
Z110402010101 TWO–DIMENSIONAL LINEAR–ARRAY TRANSCUTANEOUS ULTRASOUND PROBES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Denmark 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

Category: Extracorporeal ultrasound imaging transducer, hand-held

L13-6 by Fujifilm Sonosite, Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Extracorporeal ultrasound imaging transducer, hand-held.

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 08f5fcef-2291-43ee-959d-41249209833c 61 fields · synced Jun 18, 2026