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INTRODUTTORE/DILATATORE PEEL-AWAY 13F(13, 5/17cm)

by Med Italia Biomedica S.R.L

Ref 852073Model DISPOSITIVI E ACCESSORI PER ACCESSO PERCUTANEO IN TECHNICHE DI CATETERIZZAZIONE

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-852073QX Basic UDI-DI D-852073QXUDI-DIDate29 Jun 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  • Withdrawn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
INTRODUTTORE/DILATATORE PEEL-AWAY 13F(13,5/17cm)
Model / Reference
DISPOSITIVI E ACCESSORI PER ACCESSO PERCUTANEO IN TECHNICHE DI CATETERIZZAZIONE, 852073
Primary DI / UDI-DI
D-852073QX
Basic UDI-DI
B-852073QX
EMDN Code
C0503 Cardiovascular introducer sheaths, peel-away
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000025272

Other devices from Med Italia Biomedica S.R.L

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Properties

  • Sterile

Other properties (12)

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