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Dermosept

EUDAMED

Class I (EU MDR)

Ref ALGUG-26Model 500 ml

by Alg İlaç Sanayi̇ Ti̇caret Ltd. Şti̇.

Identity

Trade Name
DERMOSEPT EUDAMED
Device Name
Ultrasound Gel EUDAMED
Model / Reference
500 ml EUDAMED
ALGUG-26 EUDAMED

Identifiers

Primary DI / UDI-DI
08683020071568 EUDAMED
Basic UDI-DI
868302007156USJ60003264C EUDAMED
EMDN Code
Z11040185 ULTRASOUND SCANNERS - 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 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 adf02672-f0ff-47d9-a625-ac870ce2e5bc 61 fields · synced Jun 18, 2026