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Dermosept Eeg Paste

EUDAMED

Class I (EU MDR)

Ref ALG-EEG12Model 250 gr

by Alg İlaç Sanayi̇ Ti̇caret Ltd. Şti̇.

Identity

Trade Name
DERMOSEPT EEG PASTE EUDAMED
Device Name
DERMOSEPT EEG PASTE EUDAMED
Model / Reference
250 gr EUDAMED
ALG-EEG12 EUDAMED

Identifiers

Primary DI / UDI-DI
08697690392984 EUDAMED
Basic UDI-DI
8697690392980520220525HK EUDAMED
EMDN Code
Z12100385 ELECTROENCEPHALOGRAPHY INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Dermosept Eeg Paste by Alg İlaç Sanayi̇ Ti̇caret Ltd. Şti̇. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
TR-MF-000045198

Sources (1)

  • EUDAMED 7e31ca28-b0e2-428a-82b3-ab616d1f534b 61 fields · synced Jun 19, 2026