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Reusable Shielded Cable for detachable monopolar EMG needle electrode

EUDAMEDFDA UDI

Class I (EU MDR)

Ref TE/D54-451

by Technomed Europe

Identity

Trade Name
Reusable Shielded Cable for detachable monopolar EMG needle electrode EUDAMED
Technomed Europe FDA UDI
Generic Name
Analytical non-scalp cutaneous lead FDA UDI
Device Name
Reusable EMG cables EUDAMED
Reusable Shielded Cable, for detachable monopolar EMG needle electrode, 5 pole DIN connector FDA UDI
Model / Reference
TE/D54-451 EUDAMEDFDA UDI
Description
Reusable Shielded Cable, for detachable monopolar EMG needle electrode, 5 pole DIN connector FDA UDI

Identifiers

Primary DI / UDI-DI
08718375860960 EUDAMEDFDA UDI
Basic UDI-DI
8718375860001BZ EUDAMED
FDA Product Code
IKD FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Analytical non-scalp cutaneous lead FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
890.1175 FDA UDI
Market of Registration
Netherlands 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

Dimensions & Sizes

Size
Length — 1000 Millimeter FDA UDI

Category: Device sterilization/disinfection container, reusable

Reusable Shielded Cable for detachable monopolar EMG needle electrode by Technomed Europe — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Technomed Europe
EUDAMED SRN
NL-MF-000000064

Sources (2)

  • EUDAMED 83303eec-c122-45f5-b28f-4f1ced07b81a 61 fields · synced Jul 28, 2026
  • FDA UDI b595e3ac-1240-403e-bdda-34d837033e1e 35 fields · synced May 30, 2026