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Bonasil A+ Regular (FS) 50ml x 32

EUDAMED

Class I (EU MDR)

Ref 210105040F

by DMP Dental Industry S.A.

Identity

Trade Name
Bonasil A+ Regular (FS) 50ml x 32 EUDAMED
Device Name
Addition Curing Silicone Impression Material EUDAMED
Model / Reference
210105040F EUDAMED

Identifiers

Primary DI / UDI-DI
05206569001525 EUDAMED
Basic UDI-DI
5206569DSIL22SD EUDAMED
EMDN Code
Q01020102 DENTAL IMPRESSION VINYLSILOXANS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Greece 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

Bonasil A+ Regular (FS) 50ml x 32 by DMP Dental Industry S.A. — 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

EUDAMED SRN
GR-MF-000019283

Sources (1)

  • EUDAMED fa03eb48-d4cf-4e1b-883d-09f6fbe0276e 61 fields · synced Jun 18, 2026