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ACEMST35 /DC4

by ACEM S.p.A

Ref 111316Model ACEMST35

ACEMST35 /DC4 (111316) is a Class I device made by ACEM S.p.A, registered in EUDAMED on 14 Sep 2026 (Basic UDI-DI 805070589ACEMST35RG), active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805070589ACEMST35RG Basic UDI-DI 08050705890699UDI-DIDate14 Sep 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Lampada Scialitica
Model / reference
ACEMST35, 111316
Primary DI / UDI-DI
08050705890699
Basic UDI-DI
805070589ACEMST35RG
Direct marketing DI
08050705890699
EMDN code
Z12010701 Fixed scialytic lamps
Device class
Class I
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000022748

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See all devices from ACEM S.p.A →

Properties

Other properties (14, all answered No)