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Synek

EUDAMED

Class I (EU MDR)

Ref AH-DMXL

by Synek Med

Identity

Trade Name
SYNEK EUDAMED
Device Name
Incontinence under pads 90 X 180 EUDAMED
Model / Reference
AH-DMXL EUDAMED

Identifiers

Primary DI / UDI-DI
05944756903060 EUDAMED
Basic UDI-DI
5944756959447569AHDMXLDX EUDAMED
Direct Marketing DI
05944756903060 EUDAMED
EMDN Code
T04010299 ABSORBENT UNDERPADS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Romania 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

Synek by Synek Med — 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

Manufacturer
Synek Med
EUDAMED SRN
RO-MF-000048751

Sources (1)

  • EUDAMED 8fe14e58-cdda-4546-a2ed-10c4e5b4e5af 61 fields · synced Jun 18, 2026