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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

VISUCAT 23,8" SA — Class I MDR by IBK Systeme GmbH

MD Atlas
IBK Systeme GmbH

EUDAMED last updated this device on May 15, 2026

VISUCAT 23,8" SA

426069261V00FK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: IBK Systeme GmbH
UDI-DI code: 04260692610352
Reference / catalog number: VISUCAT 23,8" SA

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Manufacturer information

Organization name: IBK Systeme GmbH
SRN: DE-MF-000006941
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jul 13, 2023	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260692610352
Basic UDI-DI: 426069261V00FK
Reference / catalog number: VISUCAT 23,8" SA
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Sehprüfgerät mit polarisierendem 23,8" Monitor
Additional information URL: https://www.ibk-systeme.de/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q0299OPHTHALMIC DEVICES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

MultiVisus 23,8" MH426069261M00E6On the market MultiVisus 23,8" SA426069261M00E6On the market VISUCAT 23,8 MH426069261V00FKOn the market VISUCAT 32" SA426069261V00FKOn 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.