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Duplo

EUDAMED

Class I (EU MDR)

Ref 6073.2Ref 6073.3

by Laboratorios Herbitas, S.l.

Identity

Trade Name
DUPLO EUDAMED
Device Name
TALONERA DUPLO EUDAMED
Model / Reference
6073.2 EUDAMED
6073.3 EUDAMED

Identifiers

Primary DI / UDI-DI
08435135500439 EUDAMED
08435135500446 EUDAMED
Basic UDI-DI
84351355DUPLOQ9 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

Duplo 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 (2)

  • EUDAMED 01f2875e-fbda-41b4-9af4-593debfc3ccb 61 fields · synced Jul 31, 2026
  • EUDAMED 3885e87f-7f94-4bf5-b598-16d8de4c61a6 61 fields · synced May 19, 2026