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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

30183889 — IVDR Class A IVDR by Tecan Austria GmbH

MD Atlas
Tecan Austria GmbH

EUDAMED last updated this device on Mar 9, 2026

30183889

912005207IVS10090000APE

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Tecan Austria GmbH
UDI-DI code: 09120052070996
Reference / catalog number: 30183889

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Manufacturer information

Organization name: Tecan Austria GmbH
SRN: AT-MF-000020241
Manufacturer status: Active

Market distribution

Primary placement in Austria; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 09120052070996
Basic UDI-DI: 912005207IVS10090000APE
Reference / catalog number: 30183889
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: https://www.tecan.com/manuals
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0201020292LIMITED PANEL IMMUNOCHEMISTRY ANALYSERS - IVD MEDICAL DEVICE SOFTWAE

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

30190374912005207IVS10080001AP4On the market 30183570912005207IVS10080000ANZOn the market 30183890912005207IVS10090000APEOn 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.