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Flexcera Base Ultra+ Pink

EUDAMED

Class I (EU MDR)

Ref RES-01-3600

by EnvisionTEC GmbH

Identity

Trade Name
Flexcera Base Ultra+ Pink EUDAMED
Device Name
Flexcera Base Ultra+ EUDAMED
Model / Reference
RES-01-3600 EUDAMED

Identifiers

Primary DI / UDI-DI
04260683220966 EUDAMED
Basic UDI-DI
426068322FLEXCERABUPLUS5U EUDAMED
Direct Marketing DI
04260683220966 EUDAMED
EMDN Code
Q010699 MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Flexcera Base Ultra+ Pink by Envisiontec 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
EnvisionTEC GmbH
EUDAMED SRN
DE-MF-000009311

Sources (1)

  • EUDAMED 87d64f41-a31c-4039-b805-8299d706236a 61 fields · synced Jul 9, 2026