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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

BHI Broth 3 ml — IVDR Class A IVDR by VIAMAR INTERNATIONAL,…

MD Atlas
VIAMAR INTERNATIONAL, s.r.o.

EUDAMED last updated this device on Jan 9, 2026

BHI Broth 3 ml

85941999298018BU

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: VIAMAR INTERNATIONAL, s.r.o.
UDI-DI code: 08594199922738
Reference / catalog number: 98396-40

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Manufacturer information

Organization name: VIAMAR INTERNATIONAL, s.r.o.
SRN: CZ-MF-000038013
Manufacturer status: Active

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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

2 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement		Still on market

Device identification

Trade name: BHI Broth 3 ml
UDI-DI code: 08594199922738
Basic UDI-DI: 85941999298018BU
Reference / catalog number: 98396-40
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 40
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)

W0104010206MEDIA IN TUBES (SOLID & LIQUID)

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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Expiration date
Manufacturing date
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Software identification