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E-connect S+

by Changzhou Sifary Medical Technology Co., Ltd.

Ref 6080258Model E-connect S+

Active European Union

CE MDR

Valid until

14 Aug 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DQS Medizinprodukte GmbH

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

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number1000328670 Date24 Sep 2026IssuedStatusActive expires 14 Aug 2029

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 1000328670 Active Amended

    Quality management system EU MDR

    Certifier
    DQS Medizinprodukte GmbH 0297
    Issued
    24 Sep 2026
    Expires
    14 Aug 2029
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Dental Root Canal Measuring and Treatment Unit
Model / Reference
E-connect S+, 6080258
Primary DI / UDI-DI
06941877800345
Basic UDI-DI
697259778EE003KU
Direct Marketing DI
06941877800345
EMDN Code
Z12110101 Dental treatment units
Device Class
Class IIa
EU market of registration
Bulgaria

Manufacturer details

EUDAMED SRN
CN-MF-000010405
Authorised representative
Caretechion GmbH DE-AR-000005946

Other devices from Changzhou Sifary Medical Technology Co., Ltd.

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Properties

  • Measuring Function

Other properties (12)

  • 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
  • Incorporates Medicinal Product: No