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Xssential Rapid Delivery Procedure Pack

by SYNDEO Medical 6 variants

Ref SYN2023Model ANG 02

Active European Union

CE MDR

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/MDR Number5065021834SYNPP009ZH Basic UDI-DI 05065024079185UDI-DIDate9 Apr 2025RegisteredStatusActive EUDAMED: not 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Angiography Pack-02
Model / Reference
ANG 02, SYN2023
Primary DI / UDI-DI
05065024079185
Basic UDI-DI
5065021834SYNPP009ZH
EMDN Code
C0104010199 Cardiac angiography diagnostic devices - other
Device Class
Class IIa
Medical Purpose
Facilitates vascular imaging and interventions with sterile instruments for angiographic procedures.

Manufacturer details

EUDAMED SRN
BE-PR-000044136

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Properties

  • Sterile