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Siftal

EUDAMED

Class I (EU MDR)

Ref 15.162.4

by Laboratorios Herbitas, S.l.

Identity

Trade Name
SIFTAL EUDAMED
Device Name
Talonera siftal cazoleta EUDAMED
Model / Reference
15.162.4 EUDAMED

Identifiers

Primary DI / UDI-DI
08435135501825 EUDAMED
Basic UDI-DI
84351355CAZOLETA2S EUDAMED
EMDN Code
Y061203 ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Orthotic insole, prefabricated, non-antimicrobial

Siftal by Laboratorios Herbitas, S.l. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthotic insole, prefabricated, non-antimicrobial.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
ES-MF-000004599

Sources (1)

  • EUDAMED fd43a511-45c7-4a3b-9839-f7ef56d08b67 61 fields · synced Jun 19, 2026