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IMAK® Compression

EUDAMED

Class I (EU MDR)

Ref A20192 Model Large

by Brownmed, Inc.

Identity

Trade Name
IMAK® Compression EUDAMED
Device Name
IMAK® Compression Arthritis Socks EUDAMED
Model / Reference
Large EUDAMED
A20192 EUDAMED

Identifiers

Primary DI / UDI-DI
06498332019274 EUDAMED
Basic UDI-DI
649833IMAKCASLGQD 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

IMAK® Compression 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 5132ca3a-185d-4ee3-ae25-a7300d2808dc 61 fields · synced May 22, 2026