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Patient Sling

EUDAMED

Class I (EU MDR)

Ref SA6391110Model Patient Sling

by Unitrend Co., Ltd.

Identity

Device Name
Patient Sling EUDAMED
Model / Reference
Patient Sling EUDAMED
SA6391110 EUDAMED

Identifiers

Primary DI / UDI-DI
04719882320217 EUDAMED
Basic UDI-DI
471988232PTSL0001BW EUDAMED
Direct Marketing DI
04719882320217 EUDAMED
EMDN Code
V0805038002 NON-RIGID SUPPORTS FOR LIFTS (HARNESSES) 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

Patient Sling by Unitrend Co., Ltd. — 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
Unitrend Co., Ltd.
EUDAMED SRN
TW-MF-000012250
Authorised Representative
KOMAS Medical Technology GmbH DE-AR-000045617

Sources (1)

  • EUDAMED a89d542c-220a-4b9b-8f19-fc15416678de 61 fields · synced Jun 19, 2026