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Universal Disconnector

EUDAMED

Class I (EU MDR)

Ref J5900.2000

by ALTATEC GmbH

Identity

Trade Name
Universal Disconnector EUDAMED
Device Name
Universal cone disconnector EUDAMED
Model / Reference
J5900.2000 EUDAMED

Identifiers

Primary DI / UDI-DI
04099797013382 EUDAMED
Basic UDI-DI
40997970006808000000000W7 EUDAMED
Secondary DI
E219J590020001 EUDAMED
EMDN Code
Z12110180 INSTRUMENTS FOR DENTAL TREATMENT UNITS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

Universal Disconnector by ALTATEC GmbH — 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
ALTATEC GmbH
EUDAMED SRN
DE-MF-000006230

Sources (1)

  • EUDAMED 902baeab-1d63-4d47-ad79-b9248d7473dd 61 fields · synced Jul 10, 2026