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byzz nxt

by orangedental GmbH & Co. KG

Ref 04260375690732

Active European Union

CE MDD

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04260375690732HT Basic UDI-DI D-04260375690732HTUDI-DIDate13 Apr 2023RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
byzz nxt
Model / Reference
04260375690732
Primary DI / UDI-DI
D-04260375690732HT
Basic UDI-DI
B-04260375690732HT
EMDN Code
V92 Medical device software - not included in other classes
Device Class
Class I
Special Device Type
-1192
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006152

From the manufacturer

Manufacturer's product page: byzz® Nxt

Other devices from orangedental GmbH & Co. KG

See all devices from orangedental GmbH & Co. KG →

Properties

  • Measuring Function

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No