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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

Löwenstein Jensen — IVDR Class A IVDR by Reactivos para…

MD Atlas
Reactivos para Diagnóstico

EUDAMED last updated this device on May 16, 2025

Löwenstein Jensen

84365422214360SF

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Reactivos para Diagnóstico
UDI-DI code: 28436542221331
Reference / catalog number: TA0168

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Manufacturer information

Organization name: Reactivos para Diagnóstico
SRN: ES-MF-000022523
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.

Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: Löwenstein Jensen
UDI-DI code: 28436542221331
Basic UDI-DI: 84365422214360SF
Reference / catalog number: TA0168
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: 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)

W0104010604MANUAL MYCOBACTERIA MEDIA (TUBES & BOTTLES)

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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