← Back to catalogue

Dermosept

EUDAMED

Class I (EU MDR)

Ref ALG UG28Model 5000 ml

by Alg İlaç Sanayi̇ Ti̇caret Ltd. Şti̇.

Identity

Trade Name
DERMOSEPT EUDAMED
Device Name
Ultrasound Gel EUDAMED
Model / Reference
5000 ml EUDAMED
ALG UG28 EUDAMED

Identifiers

Primary DI / UDI-DI
08683020070813 EUDAMED
Basic UDI-DI
868302007081USJ3000326XZ EUDAMED
Direct Marketing DI
08683020070813 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

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

Manufacturer

EUDAMED SRN
TR-MF-000045198

Sources (1)

  • EUDAMED 5ad1353d-0f32-4939-b596-10934d381ced 61 fields · synced Jun 19, 2026