← Back to catalogue

Universal Analog

EUDAMED

Class I (EU MDR)

Ref CAD-UABBLB2Model CAD-UABBLB0

by Biodenta Swiss AG

Identity

Trade Name
Universal Analog EUDAMED
Device Name
CAD-UABBLB0 EUDAMED
Model / Reference
CAD-UABBLB0 EUDAMED
CAD-UABBLB2 EUDAMED

Identifiers

Primary DI / UDI-DI
07640169735905 EUDAMED
Basic UDI-DI
0764016973CADUAVZ EUDAMED
EMDN Code
Q010280 PROSTHETIC DENTISTRY DEVICES - ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Czechia 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

Universal Analog by Biodenta Swiss AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Biodenta Swiss AG
EUDAMED SRN
CH-MF-000034374
Authorised Representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Sources (1)

  • EUDAMED f071ee8c-2103-41e6-9f86-8e1051097ae0 61 fields · synced Jun 17, 2026