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Stimulationssondenkabel Kabellänge 5 m

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 520045Model 520023

by inomed Medizintechnik GmbH

Identity

Trade Name
Stimulationssondenkabel Kabellänge 5 m EUDAMED
ISIS FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Stimulationssondenkabel monopolar, Kabellänge 3m EUDAMED
Stimulation probe cable Cable length 5 m FDA UDI
Model / Reference
520023 EUDAMED
520045 EUDAMEDFDA UDI
Description
Stimulation probe cable Cable length 5 m FDA UDI

Identifiers

Primary DI / UDI-DI
04250307609376 EUDAMEDFDA UDI
Basic UDI-DI
42503076IZC0158M EUDAMED
FDA Product Code
GWF 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
882.1870 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Orthopaedic trocar blade, reusable

Stimulationssondenkabel Kabellänge 5 m by inomed Medizintechnik GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

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

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Manufacturer

EUDAMED SRN
DE-MF-000005589

Sources (2)

  • EUDAMED 8aeef8f2-5d87-41b0-bad2-b5c04aa41157 61 fields · synced Jul 9, 2026
  • FDA UDI 144cc5a8-0f7c-4f9a-a8c6-fab107ca1ce1 33 fields · synced May 29, 2026