← Back to catalogue

Disposable Subdermal Needle Electrode, hooked

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref S50719-002

by Technomed Europe

Identity

Trade Name
Disposable Subdermal Needle Electrode, hooked EUDAMED
Neuroguard FDA UDI
Generic Name
Subdermal needle electrode FDA UDI
Device Name
Disposable Subdermal Needle Electrodes EUDAMED
Disposable Subdermal Needle Electrode, hooked, 4 x 6 colors, 2m wire, 24pcs FDA UDI
Model / Reference
S50719-002 EUDAMEDFDA UDI
Description
Disposable Subdermal Needle Electrode, hooked, 4 x 6 colors, 2m wire, 24pcs FDA UDI

Identifiers

Primary DI / UDI-DI
08720791370541 EUDAMEDFDA UDI
Basic UDI-DI
B-08720791370541 EUDAMED
FDA Product Code
GXZ FDA UDI
IKT FDA UDI
EMDN Code
N01010202 EEG EXTRACRANIC ELECTRODES EUDAMED
GMDN Term
Subdermal needle electrode FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
882.1350 FDA UDI
890.1385 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 12 Millimeter FDA UDI
Outer Diameter — 0.45 Millimeter FDA UDI
Needle Gauge — 26 Gauge FDA UDI

Disposable Subdermal Needle Electrode, hooked by Technomed Europe — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Technomed Europe
EUDAMED SRN
NL-MF-000000064

Sources (2)

  • EUDAMED 76afc1ba-009b-49ac-a222-330efa05df91 61 fields · synced Jul 9, 2026
  • FDA UDI a262bfec-6004-4c28-bc0d-efd303f4b5b3 35 fields · synced May 30, 2026