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Kit assemblato per plastica epidurale

by Advanced Medical Systems Group S.R.L. 3 variants

Ref AMS-RS/B-LOON02-SK

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 Number805424725KITEPIDUROER Basic UDI-DI 08054247250324UDI-DIDate25 Sep 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  • Withdrawn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

Device Name
Kit assemblato per plastica epidurale
Model / Reference
AMS-RS/B-LOON02-SK
Primary DI / UDI-DI
08054247250324
Basic UDI-DI
805424725KITEPIDUROER
EMDN Code
N02010101 Epiduroscopy and epiduroplastics catheters and kits
Device Class
Class IIa
Medical Purpose
Endoscopia spinale, plastica epidurale e foraminoplastica, trattamento delle stenosi spinali, trattamento farmacologico e lisi delle aderenze.

Manufacturer details

EUDAMED SRN
IT-PR-000058313

Other devices from Advanced Medical Systems Group S.R.L.

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Properties

Other properties (1)

  • Sterile: No