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Dermosept - Medium - Dermosept Yeti̇şki̇n Hasta Bezi̇-M

EUDAMED

Class I (EU MDR)

Ref ALG24-17Model M

by Alg İlaç Sanayi̇ Ti̇caret Ltd. Şti̇.

Identity

Trade Name
DERMOSEPT - MEDIUM - DERMOSEPT YETİŞKİN HASTA BEZİ-M EUDAMED
Device Name
DERMOSEPT - MEDIUM - DERMOSEPT YETİŞKİN HASTA BEZİ-M EUDAMED
Model / Reference
M EUDAMED
ALG24-17 EUDAMED

Identifiers

Primary DI / UDI-DI
08683020071681 EUDAMED
Basic UDI-DI
868302007168YHB0780327YS EUDAMED
EMDN Code
T04010199 INCONTINENCE NAPPIES - OTHER 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

Yes

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 - Medium - Dermosept Yeti̇şki̇n Hasta Bezi̇-M by Alg İlaç Sanayi̇ Ti̇caret Ltd. Şti̇. — Class I — MDR — listed in EUDAMED

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 9e92bcb3-b1f3-4d24-8053-1f5fd404d3d3 61 fields · synced Jul 14, 2026