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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

100-05000-05 — IVDR Class A IVDR by I.T.A.-Intertact s.r.o.

MD Atlas
I.T.A.-Intertact s.r.o.

EUDAMED last updated this device on May 15, 2026

100-05000-05

859421827FXL05000WQ

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: I.T.A.-Intertact s.r.o.
UDI-DI code: 08594218270024
Reference / catalog number: 100-05000-05

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Manufacturer information

Organization name: I.T.A.-Intertact s.r.o.
SRN: CZ-MF-000003664
Manufacturer status: Active

Critical warnings

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

CW043
EUDAMED did not publish a description for this code.
CW044
EUDAMED did not publish a description for this code.
CW076
EUDAMED did not publish a description for this code.
CW080
EUDAMED did not publish a description for this code.
CW082
EUDAMED did not publish a description for this code.
CW083
EUDAMED did not publish a description for this code.
CW085
EUDAMED did not publish a description for this code.
CW088
EUDAMED did not publish a description for this code.
CW093
EUDAMED did not publish a description for this code.
CW094
EUDAMED did not publish a description for this code.
CW100
Eye
CW137
EUDAMED did not publish a description for this code.
CW138
EUDAMED did not publish a description for this code.
CW158
EUDAMED did not publish a description for this code.
CW162
EUDAMED did not publish a description for this code.
CW163
EUDAMED did not publish a description for this code.
CW164
EUDAMED did not publish a description for this code.
CW165
EUDAMED did not publish a description for this code.
CW167
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Czechia; available across 2 countries total.

Country	On market since	Until
CzechiaPrimary placement	Jan 30, 2024	Still on market
Slovakia	Jan 30, 2024	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08594218270024
Basic UDI-DI: 859421827FXL05000WQ
Reference / catalog number: 100-05000-05
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)

W0103080599AUXILIARY & SUPPLEMENTAL REAGENTS FOR FLOW CYTOMETRY - OTHER

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

164620859421827AFDF164620BFOn the market 100-05000-02859421827FXFW05000K7On the market 100-05000-01859421827FXFW05000K7On the market 100-05000-03859421827FXFWF05000CDOn the market 100-05000-04859421827FXFWF05000CDOn 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.