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RevoFit® Lamination Kit with Click® Reel

EUDAMED

Class I (EU MDR)

Ref RF-200-07-01

by Click Medical LLC

Identity

Trade Name
RevoFit® Lamination Kit with Click® Reel EUDAMED
Device Name
RevoFit and RevoSurface Kits EUDAMED
Model / Reference
RF-200-07-01 EUDAMED

Identifiers

Primary DI / UDI-DI
00850028855003 EUDAMED
Basic UDI-DI
0850028855PK200032097 EUDAMED
EMDN Code
Y0699 EXTERNAL PROSTHESES AND ORTHOSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

RevoFit® Lamination Kit with Click® Reel by Click Medical LLC — 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
Click Medical LLC
EUDAMED SRN
US-MF-000031805
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED cc4344bc-2365-4cea-882e-c425f203102b 61 fields · synced Jun 18, 2026