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Grid-/TES-Stimulationsmatrix 8 Ch. an ISIS Neurostimulator

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 540559Ref 540549Model 540501

by inomed Medizintechnik GmbH

Identity

Trade Name
Grid-/TES-Stimulationsmatrix 8 Ch. an ISIS Neurostimulator EUDAMED
ISIS FDA UDI
Generic Name
Nerve-function monitor FDA UDI
Device Name
Grid-/TES-Stimulationsmatrix EUDAMED
SEP-Stimulationsadapter an ISIS Neurostimulator EUDAMED
Grid/TES Stimulation matrix 8 Ch. for ISIS Neurostimulator (LED) FDA UDI
Model / Reference
540559 EUDAMEDFDA UDI
540501 EUDAMED
540549 EUDAMED
Description
Grid/TES Stimulation matrix 8 Ch. for ISIS Neurostimulator (LED) FDA UDI

Identifiers

Primary DI / UDI-DI
04250307609130 EUDAMEDFDA UDI
04250307604685 EUDAMED
Basic UDI-DI
42503076IZB0608K EUDAMED
42503076IZB02087 EUDAMED
FDA Product Code
GWF FDA UDI
EMDN Code
Z12109080 VARIOUS NEUROLOGY AND NEUROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Nerve-function monitor 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

Grid-/TES-Stimulationsmatrix 8 Ch. an ISIS Neurostimulator 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

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Manufacturer

EUDAMED SRN
DE-MF-000005589

Sources (3)

  • EUDAMED 1fffa71e-114b-4f4c-b075-5176c1e9447c 61 fields · synced Jul 26, 2026
  • FDA UDI aca5d899-2370-4653-b49b-3377e6fd8f46 33 fields · synced May 30, 2026
  • EUDAMED 3bf5c001-bbd8-4213-9b10-506f3c516db8 61 fields · synced Jul 16, 2026