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Ultrasound Fetal transducer

EUDAMED

Class IIa (EU MDR)

Ref FUS-PH02

by Orantech Inc.

Identity

Trade Name
Ultrasound Fetal transducer EUDAMED
Device Name
Ultrasound Fetal transducer EUDAMED
Model / Reference
FUS-PH02 EUDAMED

Identifiers

Primary DI / UDI-DI
06970706360392 EUDAMED
Basic UDI-DI
B-06970706360392 EUDAMED
EMDN Code
Z12080101 FOETAL MONITORS 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Ultrasound Fetal transducer by Orantech Inc. — Class IIa — 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

Manufacturer
Orantech Inc.
EUDAMED SRN
CN-MF-000013859
Authorised Representative
Medten EU ApS DK-AR-000034434

Sources (1)

  • EUDAMED 4baa5507-1482-4a03-b757-5b7753cd1262 61 fields · synced Jun 18, 2026