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Sequential Compression Sleeves

EUDAMED

Class I (EU MDR)

Ref LBTK501Model LBTK500-S

by Dalian Labtek Science & Development Co., Ltd.

Identity

Trade Name
Sequential Compression Sleeves EUDAMED
Device Name
Sequential Compression Sleeves EUDAMED
Model / Reference
LBTK500-S EUDAMED
LBTK501 EUDAMED

Identifiers

Primary DI / UDI-DI
06971599072102 EUDAMED
Basic UDI-DI
697159907SCS-LBTKXXXXX7X EUDAMED
EMDN Code
M030405 COMPRESSION STOCKINGS 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

Category: Compression/pressure sock/stocking, single-use

Sequential Compression Sleeves by Dalian Labtek Science & Development Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000042341
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 2dc70a80-14be-4a2d-86de-4e4fce66d403 61 fields · synced Jun 18, 2026