Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

Salmonella Antiserum H:z - 1ml — IVDR Class A IVDR

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

EUDAMED last updated this device on Mar 5, 2025

Salmonella Antiserum H:z - 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: 05905753742991
Reference / catalog number: SH093

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

View device family (Basic UDI)

Manufacturer information

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

Related devices

SIT OH-Sal Kit Quick Identification Test for in vitro diagnostic of Salmonella spp.590575374PS006FAOn the market Rabbit coagulase plasma (lyophilized) - 2ml590575374OSO002KDOn the market Rabbit coagulase plasma (lyophilized) - 5ml590575374OSO002KDOn the market Salmonella Antiserum H:1 - 1ml590575374SAL001E4On the market Salmonella Antiserum H:1 - 2ml590575374SAL001E4On the market

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.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

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:z - 1ml
UDI-DI code: 05905753742991
Basic UDI-DI: 590575374SAL001E4
Reference / catalog number: SH093
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
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05905753742991

Sign in to download the DataMatrix

Create a free account to download the UDI-DI DataMatrix for this device.

Email

Password

No account yet?

UDI-PI DataMatrix

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

Sign in to generate the UDI-PI DataMatrix

Create a free account, then generate the compliant UDI-PI carrier for this device.

Email

Password

No account yet?

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

Become a partner of MD Atlas

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.