Bonascan Heavy (RS) 50ml x 100

by DMP Dental Industry S.A.

Ref 210121070

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number5206569DSIL22SD Basic UDI-DI 05206569009538UDI-DI	Date21 May 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Addition Curing Silicone Impression Material
Model / Reference: 210121070

Primary DI / UDI-DI: 05206569009538
Basic UDI-DI: 5206569DSIL22SD
EMDN Code: Q01020102 Dental impression vinylsiloxans

Device Class: Class I
EU market of registration: Greece

Manufacturer details

EUDAMED SRN: GR-MF-000019283

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Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No