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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

MFG020002 — IVDD — General IVDD by BGI EUROPE A/S

MD Atlas
BGI EUROPE A/S

EUDAMED last updated this device on May 21, 2026

MFG020002

B-05745000468065

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: BGI EUROPE A/S
UDI-DI code: 05745000468065
Reference / catalog number: MFG020002

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Manufacturer information

Organization name: BGI EUROPE A/S
SRN: DK-MF-000014089
Manufacturer status: Active

Related devices

MFG020003B-05745000468072On the market MFG030008B-05745000468126On the market MFG02001B-05745000468119On the market MFG030009B-05745000468133On the market MFG030007B-05745000468096On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Denmark; available across 1 country total.

Country	On market since	Until
DenmarkPrimary placement	Dec 7, 2021	May 21, 2026

Device identification

Trade name: not provided
UDI-DI code: 05745000468065
Basic UDI-DI: B-05745000468065
Reference / catalog number: MFG020002
Issuing entity: GS1

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0105041003PARTIAL GENOTYPING HIGH-RISK HPV - NA REAGENTS

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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