Skip to content

Nostrum

by Envision Scientific Pvt. Ltd. 74 variants

Ref ENO30052

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDD, withdrawn

Ended

Withdrawn

Date not published (CE MDD)

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/MDD NumberB-08906061903002 Basic UDI-DI 08906061903002UDI-DIDate7 Aug 2026RegisteredStatusWithdrawn No longer placed on the EU market

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  • Withdrawn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European Union — CE/MDD Withdrawn

Specification

EUDAMED

Device Name
Nostrum Sirolimus Eluting Coronary Stent System
Model / Reference
ENO30052
Primary DI / UDI-DI
08906061903002
Basic UDI-DI
B-08906061903002
EMDN Code
P070402010301 Coronary drug eluting stents (des) with polymers
Device Class
Class III

Manufacturer details

EUDAMED SRN
IN-MF-000013319
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Envision Scientific Pvt. Ltd.

See all devices from Envision Scientific Pvt. Ltd. →

Properties

  • Sterile
  • Implantable
  • Administering Medicine
  • Incorporates Medicinal Product

Other properties (7)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Measuring Function: No