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KIT PER TORA-PARACENTESI AGO di VERRES 18G SACCA 2000 ML con rubinetto di scarico connettore per sacca ricambio

by Meika Group S.r.l.

Ref TOR0209Model TORAFLEX

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08055348434446 Basic UDI-DI 08055348434446UDI-DIDate11 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  • Withdrawn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
KIT PER TORA-PARACENTESI AGO di VERRES 18G SACCA 2000 ML con rubinetto di scarico connettore per sacca ricambio
Model / Reference
TORAFLEX, TOR0209
Primary DI / UDI-DI
08055348434446
Basic UDI-DI
B-08055348434446
EMDN Code
A060204 Thoracentesis and paracentesis drainages and kits
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000029106

Other devices from Meika Group S.r.l.

See all devices from Meika Group S.r.l. →

Properties

  • Sterile

Other properties (10)

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