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Kinetic Finger Sleeve

EUDAMED

Class I (EU MDR)

Ref 40430Model Universal

by Brownmed, Inc.

Identity

Trade Name
Kinetic Finger Sleeve EUDAMED
Device Name
Spark® Kinetic Finger Sleeve EUDAMED
Model / Reference
Universal EUDAMED
40430 EUDAMED

Identifiers

Primary DI / UDI-DI
00082161404309 EUDAMED
Basic UDI-DI
082161SPARKKFSCS EUDAMED
EMDN Code
M0304010101 ELASTIC COMPRESSION BANDAGES, NON-ADHESIVE, LOW EXTENSIBILITY (<70%) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Kinetic Finger Sleeve by Brownmed, 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

Manufacturer
Brownmed, Inc.
EUDAMED SRN
US-MF-000008271
Authorised Representative
AR Experts B.V. NL-AR-000023989

Sources (1)

  • EUDAMED a68b9d2d-c48e-431d-945b-f528f674903d 61 fields · synced Jun 19, 2026