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HERMETIC Powder

EUDAMED

Class IIa (EU MDR)

Ref 0032309

by lege artis Pharma GmbH + Co. KG

Identity

Device Name
HERMETIC Powder EUDAMED
Model / Reference
0032309 EUDAMED

Identifiers

Primary DI / UDI-DI
111669976960 EUDAMED
Basic UDI-DI
B-111669976960 EUDAMED
EMDN Code
Q0101010202 ROOT CANAL CEMENTS 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

HERMETIC Powder by lege artis Pharma GmbH + Co. KG — 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

EUDAMED SRN
DE-MF-000006175

Sources (1)

  • EUDAMED ac477ba7-dc9f-4367-9044-1bf85b0c839f 61 fields · synced Oct 9, 2026