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Alstringent

EUDAMED

Class I (EU MDR)

Ref ALST20Model Astringent solution

by Alan & Co

Identity

Trade Name
Alstringent EUDAMED
Device Name
Alstringent EUDAMED
Model / Reference
Astringent solution EUDAMED
ALST20 EUDAMED

Identifiers

Primary DI / UDI-DI
05425032540181 EUDAMED
Basic UDI-DI
542503254ALST7X EUDAMED
EMDN Code
Q019007 BUCCAL TOPICAL TREATMENT PREPARATIONS NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium 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

Alstringent by Alan & Co — 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
Alan & Co
EUDAMED SRN
BE-MF-000000141

Sources (1)

  • EUDAMED a3cdcf08-5877-4dea-a0ab-6b75e7f37a9b 61 fields · synced Jun 20, 2026