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ReBorn

by Lightfective Ltd. Israel EUDAMED

Ref ReBorn SystemModel ReBorn

EMDN V9099

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7290019883RBHU Basic UDI-DIDate11 May 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
ReBorn System
Model / Reference
ReBorn, ReBorn System
Primary DI / UDI-DI
07290019883005
Basic UDI-DI
7290019883RBHU
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
IL-MF-000046904
Authorised representative
G&D&Y NL-AR-000013751

Related devices

Category: Device sterilization/disinfection container, reusable

Other devices from Lightfective, Ltd.

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 13dbd622-d5a5-4123-9330-f48ec1884d7b 61 fields · synced 22 Oct 2026