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Patient Sling

EUDAMED

Class I (EU MDR)

Ref SR3701000Model Patient SlingRef SA6391100Ref SR3702000Ref RP881Ref SA6391500

by Unitrend Co., Ltd.

Identity

Device Name
Patient Sling EUDAMED
Model / Reference
Patient Sling EUDAMED
SR3701000 EUDAMED
SA6391100 EUDAMED
SR3702000 EUDAMED
RP881 EUDAMED
SA6391500 EUDAMED

Identifiers

Primary DI / UDI-DI
04719882320002 EUDAMED
04719882320033 EUDAMED
04719882320453 EUDAMED
04719882320583 EUDAMED
04719882320019 EUDAMED
Basic UDI-DI
471988232PTSL0001BW EUDAMED
Direct Marketing DI
04719882320002 EUDAMED
04719882320033 EUDAMED
04719882320453 EUDAMED
04719882320583 EUDAMED
04719882320019 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 (5)

  • EUDAMED 81631c37-596b-4816-b7ad-122df02f0f21 61 fields · synced Jul 30, 2026
  • EUDAMED ecd11980-e553-448f-a96f-675a20698f06 61 fields · synced May 17, 2026
  • EUDAMED 3a8fd761-399b-45a2-a2e3-b484de2c4ded 61 fields · synced May 18, 2026
  • EUDAMED 78ff1170-3cfe-475f-8173-9f2791602b41 61 fields · synced May 18, 2026
  • EUDAMED 95168c98-bb2d-466e-b90f-be433742fd95 61 fields · synced May 19, 2026