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Multiplus

EUDAMED

Class I (EU MDR)

Ref ALG UG29Model 250 ml

by Alg İlaç Sanayi̇ Ti̇caret Ltd. Şti̇.

Identity

Trade Name
MULTIPLUS EUDAMED
Device Name
Ultrasound Gel EUDAMED
Model / Reference
250 ml EUDAMED
ALG UG29 EUDAMED

Identifiers

Primary DI / UDI-DI
08697690393769 EUDAMED
Basic UDI-DI
869769039376ALG2500626SP EUDAMED
Direct Marketing DI
08697690393769 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

Multiplus 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 1583a5f9-6843-4d2e-818b-6df4378040ce 61 fields · synced Jun 18, 2026