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Patient Cable

EUDAMED

Class I (EU MDR)

Ref IFC-GE01-15

by Orantech Inc.

Identity

Trade Name
Patient Cable EUDAMED
Device Name
Patient Cable EUDAMED
Model / Reference
IFC-GE01-15 EUDAMED

Identifiers

Primary DI / UDI-DI
06941691985457 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

Category: General-purpose multi-parameter bedside monitor

Patient Cable by Orantech Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose multi-parameter bedside monitor.

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 e580e2c5-31e4-4221-8948-801132924697 61 fields · synced May 23, 2026