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BARILUX OG Calibration Tube

EUDAMED

Class IIa (EU MDR)

Ref NL03-01Model 34FR,36FR,38FR,40FR

by Suzhou Anying Medical Equipment Co., Ltd

Identity

Trade Name
BARILUX OG Calibration Tube EUDAMED
Single Use Sterile BARILUX OG Calibration Tube EUDAMED
Device Name
BARILUX OG Calibration Tube EUDAMED
Single Use Sterile BARILUX OG Calibration Tube EUDAMED
Model / Reference
34FR,36FR,38FR,40FR EUDAMED
NL03-01 EUDAMED

Identifiers

Primary DI / UDI-DI
06978494522343 EUDAMED
Basic UDI-DI
697849452WG23042501Q7 EUDAMED
Direct Marketing DI
06978494522343 EUDAMED
EMDN Code
G020502 GASTRIC CALIBRATION TUBES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

Yes

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

BARILUX OG Calibration Tube by Suzhou Anying Medical Equipment Co., Ltd — Class IIa — 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-000047126
Authorised Representative
Llins Service & Consulting GmbH DE-AR-000009077

Sources (2)

  • EUDAMED 00fbbf47-596a-42e9-a224-808940185c35 61 fields · synced Jun 20, 2026
  • EUDAMED b73d55c3-0b1f-4100-8c69-17d3f577f6d2 61 fields · synced Jun 20, 2026