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Glasiosite

EUDAMED

Class IIa (EU MDR)

Ref 1601Model caps

by VOCO GmbH

Identity

Trade Name
Glasiosite EUDAMED
Device Name
Glasiosite EUDAMED
Model / Reference
caps EUDAMED
1601 EUDAMED

Identifiers

Primary DI / UDI-DI
E22116011 EUDAMED
Basic UDI-DI
B-E22116011 EUDAMED
EMDN Code
Q01010105 DENTAL RESTORATION COMPOMERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Glasiosite by VOCO GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
VOCO GmbH
EUDAMED SRN
DE-MF-000008601

Sources (1)

  • EUDAMED 7ba52eea-bb36-42e1-904f-c90d26f6e601 61 fields · synced Jul 13, 2026