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ArmaResin PERMANENT TOUGH A2 500 gr

by Arma Dental Üreti̇m Si̇stemleri̇ San.ve Ti̇c.ltd.şti̇.

Ref ADPA20-0500-TH

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number86843826ARPT2A Basic UDI-DI 08684382607440UDI-DIDate4 Jun 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
ArmaResin PERMANENT TOUGH
Model / Reference
ADPA20-0500-TH
Primary DI / UDI-DI
08684382607440
Basic UDI-DI
86843826ARPT2A
Direct Marketing DI
08684382607440
EMDN Code
Q0102050199 Dentistry resins - other
Device Class
Class IIa
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000036993

Other devices from Arma Dental Üreti̇m Si̇stemleri̇ San.ve Ti̇c.ltd.şti̇.

See all devices from Arma Dental Üreti̇m Si̇stemleri̇ San.ve Ti̇c.ltd.şti̇. →

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