← Back to catalogue

Dermosept - Large - Dermosept Yeti̇şki̇n Hasta Bezi̇

EUDAMED

Class I (EU MDR)

Ref ALG24-19Model L

by Alg İlaç Sanayi̇ Ti̇caret Ltd. Şti̇.

Identity

Trade Name
DERMOSEPT - LARGE - DERMOSEPT YETİŞKİN HASTA BEZİ EUDAMED
Device Name
DERMOSEPT - LARGE - DERMOSEPT YETİŞKİN HASTA BEZİ EUDAMED
Model / Reference
L EUDAMED
ALG24-19 EUDAMED

Identifiers

Primary DI / UDI-DI
08683020071698 EUDAMED
Basic UDI-DI
868302007169YHB0760327Z3 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 - Large - Dermosept Yeti̇şki̇n Hasta Bezi̇ 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 803a45a1-2320-4bde-9a30-f71f7c2f1905 61 fields · synced Jul 9, 2026