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Toro

by Deka M.E.L.A. SRL 3 variants

Ref M136A1

Toro (M136A1) is a Class IIb device made by Deka M.E.L.A. SRL, registered in EUDAMED on 17 Mar 2025 (Basic UDI-DI 803410851M136A1B1MZ), 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803410851M136A1B1MZ Basic UDI-DI 08034108512617UDI-DIDate17 Mar 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
M136A1
Primary DI / UDI-DI
08034108512617
Basic UDI-DI
803410851M136A1B1MZ
EMDN code
Z12011017 Neodymium surgical laser
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000007389

Similar devices in this category

Other devices filed under NEODYMIUM SURGICAL LASER.

Other devices from Deka M.E.L.A. SRL

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Properties

  • Sterilise before use
Other properties (13, all answered No)