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Zerosole

EUDAMED

Class I (EU MDR)

Ref ZS001Model Reliever

by Kaydiar Medical

Identity

Trade Name
ZEROSOLE EUDAMED
Device Name
ZeroSole EUDAMED
Model / Reference
Reliever EUDAMED
ZS001 EUDAMED

Identifiers

Primary DI / UDI-DI
05070002162810 EUDAMED
05070002162803 EUDAMED
Basic UDI-DI
507000216ZSRelieverQY EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Zerosole by Kaydiar Medical — 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

Manufacturer
Kaydiar Medical
EUDAMED SRN
UK-MF-000043517
Authorised Representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Sources (2)

  • EUDAMED 1d2eca4f-2e98-495b-994a-09fb9ad4908e 61 fields · synced Jul 22, 2026
  • EUDAMED 1b249375-e611-409f-822f-ae91228c0713 61 fields · synced May 19, 2026