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Amalgam Well

EUDAMED

Class I (EU MDR)

Ref DI-03-910

by Zasber International

Identity

Trade Name
Amalgam Well EUDAMED
Device Name
Amalgam Well EUDAMED
Model / Reference
DI-03-910 EUDAMED

Identifiers

Primary DI / UDI-DI
08964004873614 EUDAMED
Basic UDI-DI
8964004873614DI03910P8 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Category: Device sterilization/disinfection container, reusable

Amalgam Well by Zasber International — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
PK-MF-000046743
Authorised Representative
Yousfis S.L. ES-AR-000041900

Sources (1)

  • EUDAMED eae551b6-a3cd-4348-9ed2-d22651958f8e 61 fields · synced Aug 1, 2026