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Permlastic

EUDAMED

Class I (EU MDR)

Ref 60102

by Kerr Italia Srl

Identity

Device Name
Permlastic EUDAMED
Model / Reference
60102 EUDAMED

Identifiers

Primary DI / UDI-DI
08055165041902 EUDAMED
Basic UDI-DI
80515118710000134Z EUDAMED
EMDN Code
Q01020199 DENTAL IMPRESSION MATERIALS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Permlastic by Kerr Italia Srl — 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
Kerr Italia Srl
EUDAMED SRN
IT-MF-000007768

Sources (1)

  • EUDAMED a1d20b10-591d-4e11-abd4-f98959245388 61 fields · synced Jul 20, 2026