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Regulator

EUDAMED

Class I (EU MDR)

Ref BXR03Model BXR01、BXR02、BXR03

by Hebei Boxin Recovery Equipment CO., LTD

Identity

Device Name
Regulator EUDAMED
Model / Reference
BXR01、BXR02、BXR03 EUDAMED
BXR03 EUDAMED

Identifiers

Primary DI / UDI-DI
06971408229727 EUDAMED
Basic UDI-DI
697140822R01M2 EUDAMED
EMDN Code
A030104 FLOW REGULATORS 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

Regulator by Hebei Boxin Recovery Equipment 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-000046611
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED cc4f1288-84c0-467d-9733-dd065fa13b7a 61 fields · synced Jun 19, 2026