← Back to catalogue

Duplo

EUDAMED

Class I (EU MDR)

Ref 6073.1

by Laboratorios Herbitas, S.l.

Identity

Trade Name
DUPLO EUDAMED
Device Name
TALONERA DUPLO EUDAMED
Model / Reference
6073.1 EUDAMED

Identifiers

Primary DI / UDI-DI
08435135500422 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
ES-MF-000004599

Sources (1)

  • EUDAMED 578b5d6d-46e1-4b61-9f9a-e09dffc33b0a 61 fields · synced Jun 18, 2026