← Back to catalogue

Blanda Blanda

EUDAMED

Class I (EU MDR)

Ref 10.025.3

by Laboratorios Herbitas, S.l.

Identity

Trade Name
BLANDA BLANDA EUDAMED
Device Name
Ortesis Podológicas EUDAMED
Model / Reference
10.025.3 EUDAMED

Identifiers

Primary DI / UDI-DI
08435135515389 EUDAMED
Basic UDI-DI
84351355BLANDAGJ 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

Blanda Blanda 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 c9d79df9-6ae8-4456-ab16-8a10dce0e30d 61 fields · synced Jun 19, 2026