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Viar-Rx-N

by AR Baltic Medical UAB 69 variants

Ref VIAR-RX-N 30225

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04772085013652 Basic UDI-DI 04772085013652UDI-DIDate17 Aug 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

LithuaniaGermanyHungaryBulgariaSpainItaly
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

  • Bulgaria
  • Germany
  • Hungary
  • Italy
  • Lithuania
  • Spain

Specification

EUDAMED

Device Name
Balloon catheter VIAR
Model / Reference
VIAR-RX-N 30225
Primary DI / UDI-DI
04772085013652
Basic UDI-DI
B-04772085013652
EMDN Code
C010402020101 PTA balloon dilatation catheters
Device Class
Class III
EU market of registration
Lithuania

Manufacturer details

EUDAMED SRN
LT-MF-000004402

Other devices from AR Baltic Medical UAB

See all devices from AR Baltic Medical UAB →

Properties

  • Sterile

Other properties (10)

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