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Kruidvat

EUDAMED

Class I (EU MDR)

Ref KV-1119009 V2

by Aso Philippines, Inc.

Identity

Trade Name
Kruidvat EUDAMED
Device Name
Neoprene Bandage Wrist / Ankle / Knee EUDAMED
Model / Reference
KV-1119009 V2 EUDAMED

Identifiers

Primary DI / UDI-DI
08719179627285 EUDAMED
Basic UDI-DI
48079990API081N9 EUDAMED
EMDN Code
Y061209 KNEE ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Kruidvat by Aso Philippines, Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
PH-MF-000027714
Authorised Representative
Aso Europe BV NL-AR-000004377

Sources (1)

  • EUDAMED 7ea6ac81-df7d-43ed-a337-004096c6966a 61 fields · synced Jul 9, 2026