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Siftal

by Laboratorios Herbitas, S.L. 13 variants

Ref 15.162.4

Siftal (15.162.4) is a Class I device made by Laboratorios Herbitas, S.L., registered in EUDAMED on 5 Nov 2024 (Basic UDI-DI 84351355CAZOLETA2S), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number84351355CAZOLETA2S Basic UDI-DI 08435135501825UDI-DIDate5 Nov 2024RegisteredStatusActive

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  • Withdrawn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
Talonera siftal cazoleta
Model / reference
15.162.4
Primary DI / UDI-DI
08435135501825
Basic UDI-DI
84351355CAZOLETA2S
EMDN code
Y061203 Orthoses, foot (including insoles and inserts)
Device class
Class I
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000004599

Similar devices in this category

Other devices filed under ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS).

Other devices from Laboratorios Herbitas, S.L.

See all devices from Laboratorios Herbitas, S.L. →

Properties

Other properties (14, all answered No)