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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

Dynasit LIFE+ — Class I MDR by Mlad s.r.o.

MD Atlas
Mlad s.r.o.

EUDAMED last updated this device on May 26, 2026

Dynasit LIFE+

8588010830DYNZRES

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Mlad s.r.o.
UDI-DI code: 08588010830029
Reference / catalog number: K92349

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View device family (Basic UDI)

Manufacturer information

Organization name: Mlad s.r.o.
SRN: SK-MF-000054470
Manufacturer status: Active

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: Dynasit LIFE+
UDI-DI code: 08588010830029
Basic UDI-DI: 8588010830DYNZRES
Reference / catalog number: K92349
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: Dynasit LIFE+ – dual-chamber dynamic inflatable seating cushion intended to support active and ergonomic sitting. The dual-chamber system provides enhanced sitting dynamics, supports body micro-movements during sitting and activation of stabilizing muscles. Helps reduce pressure on intervertebral disc spaces, supports blood circulation and may contribute to improved mental focus and sitting comfort during work or prolonged sitting.
Additional information URL: https://www.dynasit.sk/user/documents/upload/Pribalovy%20letak.pdf
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)08588010830029

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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.

V080302PATIENT POSITIONING MEDICAL CUSHIONS

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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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.