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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

Salmonella Antiserum H:f,g - 1ml — IVDR Class A IVDR

MD Atlas
Zakład Badawczo-Wdrożeniowy Ośrodka Salmonella "IMMUNOLAB" Sp. z o. o.

EUDAMED last updated this device on Jul 18, 2025

Salmonella Antiserum H:f,g - 1ml

590575374SAL001E4

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Zakład Badawczo-Wdrożeniowy Ośrodka Salmonella "IMMUNOLAB" Sp. z o. o.
UDI-DI code: 05905753741956
Reference / catalog number: SH068

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Manufacturer information

Organization name: Zakład Badawczo-Wdrożeniowy Ośrodka Salmonella "IMMUNOLAB" Sp. z o. o.
SRN: PL-MF-000042563
Manufacturer status: Active

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Critical warnings

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

CW267
Rabbit antisera contain material of animal origin and should be handled as potentially infectious.

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Market distribution

Primary placement in Poland; available across 1 country total.

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

Device identification

Trade name: Salmonella Antiserum H:f,g - 1ml
UDI-DI code: 05905753741956
Basic UDI-DI: 590575374SAL001E4
Reference / catalog number: SH068
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: The antisera for Salmonella slide agglutination assay are an in vitro diagnostic medical device. The antisera are used for qualitative identification tests of Salmonella serotypes isolated on bacteriological media from human or animal samples or other materials.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
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Manufacturing date
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Software identification

UDI-DI DataMatrix

Encoded

(01)05905753741956

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

W0104080301SEROTYPING (E.COLI, SALMONELLA, SHIGELLA, ETC)

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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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.