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Technomed Europe

FDA UDI

Class II (US FDA UDI)

by Technomed Engineering B.V.

Identity

Trade Name
Technomed Europe FDA UDI
Generic Name
Analytical scalp electrode, reusable FDA UDI
Device Name
Reusable EEG Cup Electrode Silver/Silver Chloride (Ag/AgCl), 12 pieces FDA UDI
Model / Reference
TE/C24-434/99 FDA UDI
Description
Reusable EEG Cup Electrode Silver/Silver Chloride (Ag/AgCl), 12 pieces FDA UDI

Identifiers

Primary DI / UDI-DI
08718375862247 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Analytical scalp electrode, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1320 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 1 Meter FDA UDI
Outer Diameter — 6 Millimeter FDA UDI

Technomed Europe by Technomed Engineering B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 28201612-4a3d-41f0-b1b8-de2a5cef0216 36 fields · synced Jun 8, 2026