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Repin

EUDAMED

Class I (EU MDR)

Ref 4241110PE

by SpofaDental a.s.

Identity

Trade Name
Repin EUDAMED
Device Name
REPIN, 300g white paste + 125g brown paste EUDAMED
Model / Reference
4241110PE EUDAMED

Identifiers

Primary DI / UDI-DI
08594747000536 EUDAMED
Basic UDI-DI
8594747100002027 EUDAMED
EMDN Code
Q01020199 DENTAL IMPRESSION MATERIALS - OTHER 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

Category: Silicone dental impression material

Repin by SpofaDental a.s. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
SpofaDental a.s.
EUDAMED SRN
CZ-MF-000000945

Sources (1)

  • EUDAMED 089ffa68-e811-4d69-ba12-5f9255219f0e 61 fields · synced Jul 16, 2026