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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

MS — Class I MDR by AssisTech Sp. z o.o.

MD Atlas
AssisTech Sp. z o.o.

EUDAMED last updated this device on Sep 3, 2025

MS

59041628300MS5W

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AssisTech Sp. z o.o.
UDI-DI code: 05904162830084
Reference / catalog number: MS

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View device family (Basic UDI)

Manufacturer information

Organization name: AssisTech Sp. z o.o.
SRN: PL-MF-000002848
Manufacturer status: Active

Related devices

BASIC 1.059041628300MS5WOn the market BASIC 2.059041628300MS5WOn the market C-Eye59041628300CE44On the market C-Eye II59041628300CE44On the market NeuroTAB59041628300CE44On 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

No critical warnings reported for this device.

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Market distribution

Primary placement in Poland; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 05904162830084
Basic UDI-DI: 59041628300MS5W
Reference / catalog number: MS
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: A mobile stand allows the device (C-Eye) to be positioned at any angle and at the right distance from the patient. Wheels increase the mobility of the entire set, and the especially designed base allows the device to be placed maximally close to the bed. The wheel lock option provides safety and stability.
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)05904162830084

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

Y99DEVICES FOR PERSONS WITH DISABILITIES NOT INCLUDED IN OTHER CATEGORIES - 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

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