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Dentapreg® PFU Single

EUDAMED

Class IIa (EU MDR)

Ref D-523

by ADM, a.s.

Identity

Trade Name
Dentapreg® PFU Single EUDAMED
Device Name
Dentapreg® PFU EUDAMED
Model / Reference
D-523 EUDAMED

Identifiers

Primary DI / UDI-DI
08595652700405 EUDAMED
Basic UDI-DI
85956527PFU9J EUDAMED
EMDN Code
Q010299 PROSTHETIC DENTISTRY DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Czechia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

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

Dentapreg® PFU Single by ADM, a.s. — Class IIa — 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
ADM, a.s.
EUDAMED SRN
CZ-MF-000032589

Sources (1)

  • EUDAMED 0f5afcf7-32a3-4bbd-92cd-569daeae7f08 61 fields · synced Jul 9, 2026