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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

A31533 — Class I MDR by WWW.KOMPRESS.SK, s.r.o.

MD Atlas
WWW.KOMPRESS.SK, s.r.o.

EUDAMED last updated this device on May 13, 2026

A31533

8586029160496AL

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: WWW.KOMPRESS.SK, s.r.o.
UDI-DI code: 08586029160199
Reference / catalog number: A31533

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View device family (Basic UDI)

Manufacturer information

Organization name: WWW.KOMPRESS.SK, s.r.o.
SRN: SK-MF-000053588
Manufacturer status: Active

Related devices

A31509858602916001494On the market A31505858602916001494On the market A31506858602916001494On the market A3153685860291604109GOn the market A3154385860291604279ZOn 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 Slovakia; available across 1 country total.

Country	On market since	Until
SlovakiaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08586029160199
Basic UDI-DI: 8586029160496AL
Reference / catalog number: A31533
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 20 x 30 cm

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08586029160199

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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.

M0199WOOL AND SYNTHETIC COTTON - 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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