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Organization name
UDI-DI code
Reference / catalog number

Immunofluorescence Analyzer… — IVDR Class A IVDR

MD Atlas
MP Biomedicals Germany GmbH

EUDAMED last updated this device on May 17, 2026

Immunofluorescence Analyzer MPQuanti™

42601633107IMA001J6

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: MP Biomedicals Germany GmbH
UDI-DI code: 04260163315632
Reference / catalog number: 07IMA001

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Manufacturer information

Organization name: MP Biomedicals Germany GmbH
SRN: DE-MF-000020991
Manufacturer status: Active

Critical warnings

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

CW008
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW168
Biohazard, contact test samples, calibration products, quality control products should wear gloves, otherwise it may lead to infection.
CW259
Beware of electric shock: Do not touch the internal power supply, circuit board and wire of the analyzer when it is powered on.
CW011
Indicates a danger that may cause infection.
CW999
Protective earthing

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Mar 5, 2024	Still on market
EL	Feb 2, 2024	Still on market

Device identification

Trade name: Immunofluorescence Analyzer MPQuanti™
UDI-DI code: 04260163315632
Basic UDI-DI: 42601633107IMA001J6
Reference / catalog number: 07IMA001
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)

W0201020201IMMUNOCHEMISTRY READERS

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

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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.