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SEPARADOR CARRETE silicona

EUDAMED

Class I (EU MDR)

Ref 6003.1Ref 6003.2Ref 6003.3

by Laboratorios Herbitas, S.l.

Identity

Device Name
SEPARADOR CARRETE silicona EUDAMED
Model / Reference
6003.1 EUDAMED
6003.2 EUDAMED
6003.3 EUDAMED

Identifiers

Primary DI / UDI-DI
08435135500132 EUDAMED
08435135500149 EUDAMED
08435135500156 EUDAMED
Basic UDI-DI
84351355CARRETESIL43 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

SEPARADOR CARRETE silicona 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 (3)

  • EUDAMED c9f52f4b-5ca8-42db-a1d5-979c55ec74b9 61 fields · synced Jul 12, 2026
  • EUDAMED 76376e4b-a39c-47ff-a67b-c8c4786bd3ff 61 fields · synced May 18, 2026
  • EUDAMED 059a86e8-04c7-4b0e-a92f-c5524a5cd74b 61 fields · synced May 18, 2026