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Grab bar

EUDAMED

Class I (EU MDR)

Ref FT-5203-BKModel FT-5012/FT-5016/FT-5018/FT-5024/FT-5032/FT-5000L/FT-5000R/FT-5032C/FT-5024C/FT-5018C/FT-5016C/5012C/FT-5001/FT-5002L/FT-5002R/FT-5212/FT-5216/FT-5218/FT-5224/FT-5232/FT-5236/FT-5136/FT-5132/FT-5124/FT-5118/FT-5116/FT-5112/FT-5203/FT-5204/FT-5100 etc

by Fort Metal Plastic Products (huizhou) co ., Ltd.

Identity

Device Name
Grab bar EUDAMED
Model / Reference
FT-5012/FT-5016/FT-5018/FT-5024/FT-5032/FT-5000L/FT-5000R/FT-5032C/FT-5024C/FT-5018C/FT-5016C/5012C/FT-5001/FT-5002L/FT-5002R/FT-5212/FT-5216/FT-5218/FT-5224/FT-5232/FT-5236/FT-5136/FT-5132/FT-5124/FT-5118/FT-5116/FT-5112/FT-5203/FT-5204/FT-5100 etc EUDAMED
FT-5203-BK EUDAMED

Identifiers

Primary DI / UDI-DI
06975289965668 EUDAMED
Basic UDI-DI
697528996FTGRXD EUDAMED
EMDN Code
Y181803 HANDRAILS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Grab bar by Fort Metal Plastic Products (huizhou) 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

EUDAMED SRN
CN-MF-000016919
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 2913bc29-09d0-4043-8c1b-f54f1ea34609 61 fields · synced Jun 18, 2026