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Patient Stretcher

EUDAMED

Class I (EU MDR)

Ref BT-TF019Model BT-TR001,BT-TR002,BT-TR003,BT-TR005,BT-TR006,BT-TR007,BT-TR008,BT-TR009,BT-TR010,BT-TR011,BT-TR012,BT-TR013,BT-TR014,BT-TR015,BT-TR016,BT-TR022,BT-TR023,BT-TR025, etc

by Zhangjiagang Bestran Technology Co., Ltd

Identity

Device Name
Patient Stretcher EUDAMED
Model / Reference
BT-TR001,BT-TR002,BT-TR003,BT-TR005,BT-TR006,BT-TR007,BT-TR008,BT-TR009,BT-TR010,BT-TR011,BT-TR012,BT-TR013,BT-TR014,BT-TR015,BT-TR016,BT-TR022,BT-TR023,BT-TR025, etc EUDAMED
BT-TF019 EUDAMED

Identifiers

Primary DI / UDI-DI
06977606275788 EUDAMED
Basic UDI-DI
697760627PS0001M7 EUDAMED
EMDN Code
V08050101 GENERIC USE STRETCHERS 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

Patient Stretcher by Zhangjiagang Bestran Technology 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-000042782
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 5248da19-2fb7-4154-b7d3-ec7017043903 61 fields · synced Jun 19, 2026