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MOD.M011 Aspiratore Pulsevac C/Vaso 1000R

by Spencer Italia s.r.l.

Ref SC21007Model Suction Device

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805771123SISTEMAPULSEVADP Basic UDI-DI 08057711238606UDI-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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
Suction Device, SC21007
Primary DI / UDI-DI
08057711238606
Basic UDI-DI
805771123SISTEMAPULSEVADP
EMDN Code
Z120105 Surgical medical aspirators
Device Class
Class IIa
Medical Purpose
Suction Device

Manufacturer details

EUDAMED SRN
IT-PR-000033349

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Properties

Other properties (1)

  • Sterile: No