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Infusion Pump

by Shenzhen MedRena Biotech Co., Ltd. 4 variants

Ref VP50 Pro, VP90 ProModel UniFusion VP50 Pro

Active European Union

CE MDR 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/MDR NumberB-06973586220312 Basic UDI-DI Date16 Jan 2025RegisteredStatusActive
European UnionCE/MDD NumberB-06973586220312 Basic UDI-DI Date16 Jan 2025RegisteredStatusActive

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  • Withdrawn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, CE/MDD Active

Specification

EUDAMED

Model / Reference
UniFusion VP50 Pro, VP50 Pro, VP90 Pro
Primary DI / UDI-DI
06973586220312, 06973586220718
Basic UDI-DI
B-06973586220312, 6973586222390P7N
EMDN Code
Z12030301 Infusion pumps
Device Class
Class IIb
EU market of registration
Italy
Ireland

Manufacturer details

EUDAMED SRN
CN-MF-000026006
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Shenzhen MedRena Biotech Co., Ltd.

Properties

  • Administering Medicine
  • Measuring Function NoEUDAMEDYesEUDAMED

Other properties (11)

  • 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
  • Incorporates Medicinal Product: No