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Anschlusskabel 4-Kanal für Tubus-Klebelektroden Select

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 530868Model 530663

by inomed Medizintechnik GmbH

Identity

Trade Name
Anschlusskabel 4-Kanal für Tubus-Klebelektroden Select EUDAMED
N/A FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Anschlusskabel Touchproof für Tubus-Klebeelektroden EUDAMED
Connection cable 4 channel for adhesive laryngeal electrode Select FDA UDI
Model / Reference
530663 EUDAMED
530868 EUDAMEDFDA UDI
Description
Connection cable 4 channel for adhesive laryngeal electrode Select FDA UDI

Identifiers

Primary DI / UDI-DI
04250307610020 EUDAMEDFDA UDI
Basic UDI-DI
42503076IZC0148K EUDAMED
FDA Product Code
IKD FDA UDI
EMDN Code
Z12109080 VARIOUS NEUROLOGY AND NEUROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
890.1175 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Orthopaedic trocar blade, reusable

Anschlusskabel 4-Kanal für Tubus-Klebelektroden Select by inomed Medizintechnik GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Orthopaedic trocar blade, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000005589

Sources (2)

  • EUDAMED dc448d97-deb2-445d-afae-f0ca5241d159 61 fields · synced Jul 17, 2026
  • FDA UDI 3dba802d-a800-4275-a07e-5ff4757bbdf2 33 fields · synced May 30, 2026