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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

110225 — IVDD — General IVDD by invicon diagnostic…

MD Atlas
invicon diagnostic concepts GmbH

EUDAMED last updated this device on May 12, 2026

110225

B-04260674450235

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: invicon diagnostic concepts GmbH
UDI-DI code: 04260674450235
Reference / catalog number: 110225

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View device family (Basic UDI)

Manufacturer information

Organization name: invicon diagnostic concepts GmbH
SRN: DE-MF-000031071
Manufacturer status: Active

Related devices

110249B-04260674452499On the market 110213B-04260674450198On the market 110211B-04260674450174On the market 110212B-04260674450181On the market 110231B-04260674450242On 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.

Critical warnings

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

CW011
EUDAMED did not publish a description for this code.
CW008
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW083
EUDAMED did not publish a description for this code.
CW089
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	May 19, 2005	Still on market
Austria	Dec 10, 2018	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260674450235
Basic UDI-DI: B-04260674450235
Reference / catalog number: 110225
Issuing entity: GS1

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC 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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04260674450235

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EMDN nomenclature code(s)

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

W0101050101ASSAYED MULTICOMPONENT CONTROLS (CC)

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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