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Stomaflex

EUDAMED

Class I (EU MDR)

Ref 4215330PE

by SpofaDental a.s.

Identity

Trade Name
Stomaflex EUDAMED
Device Name
STOMAFLEX PUTTY EUDAMED
Model / Reference
4215330PE EUDAMED

Identifiers

Primary DI / UDI-DI
08594747003360 EUDAMED
Basic UDI-DI
859474710000222B EUDAMED
EMDN Code
Q01020104 DENTAL IMPRESSION SILICONES 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

Stomaflex 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 3d9274ff-32a7-4f43-82c3-79ead7815a2f 61 fields · synced Jul 14, 2026