Skip to content

Iberis

by Shanghai AngioCare Medical Technology Co., Ltd. 3 variants

Ref RD*ATCB160TC

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06959582000233 Basic UDI-DI 06959582000233UDI-DIDate28 Jan 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Renal Denervation Systems
Model / Reference
RD*ATCB160TC
Primary DI / UDI-DI
06959582000233
Basic UDI-DI
B-06959582000233
EMDN Code
K02030101 Radiofrequency surgery electrodes, single-use
Device Class
Class IIb
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
CN-MF-000017311
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Shanghai AngioCare Medical Technology Co., Ltd.

Properties

  • Sterile
  • Measuring Function

Other properties (9)

  • 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