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Patient Cable

EUDAMED

Class I (EU MDR)

Ref FM-05

by Orantech Inc.

Identity

Trade Name
Patient Cable EUDAMED
Device Name
Patient Cable EUDAMED
Model / Reference
FM-05 EUDAMED

Identifiers

Primary DI / UDI-DI
06941691973386 EUDAMED
Basic UDI-DI
69416919ORANTECH24R3 EUDAMED
EMDN Code
Z1203020285 MULTI-PARAMETER MONITORS - CONSUMABLES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Denmark EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Patient Cable by Orantech 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

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

Sources (1)

  • EUDAMED 9780e125-628f-4f1a-bd36-b2ebc55e9214 61 fields · synced May 23, 2026