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eBfresh Blood Glucose Monitoring System

by Visgeneer Inc.

Ref 1320245Model eB-F01

Active European Union

CE IVDD

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-04712558769778 Basic UDI-DI 04712558769778UDI-DIDate16 Jul 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  • Withdrawn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/IVDD Active

Specification

EUDAMED

Device Name
eBfresh Blood Glucose Monitoring System
Model / Reference
eB-F01, 1320245
Primary DI / UDI-DI
04712558769778
Basic UDI-DI
B-04712558769778
EMDN Code
W0201060102 Blood glucose meters
Device Class
Class IVD devices for self-testing
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
TW-MF-000036547
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from Visgeneer, Inc.

See all devices from Visgeneer, Inc. →

Properties

  • Microbial Substances
  • Self Testing
  • Near-Patient Testing
  • Professional Testing

Other properties (6)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Reagent: No
  • Companion Diagnostics: No
  • Surgical Instrument: No