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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

System with "Venturi" type… — Class IIa MDR by MEDES S.r.l.

MD Atlas
MEDES S.r.l.

EUDAMED last updated this device on Apr 24, 2026

System with "Venturi" type ejectors in the terminal units

805759237MAGSSJG

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDES S.r.l.
UDI-DI code: 08057592370129
Reference / catalog number: System with "Venturi" type ejectors in the terminal units

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View device family (Basic UDI)

Manufacturer information

Organization name: MEDES S.r.l.
SRN: IT-MF-000025275
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

042-00-02-MDRSupplemented
Quality management systemNotified body: 0426Expiry: Feb 19, 2029

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 2 countries total.

Country	On market since	Until
ItalyPrimary placement		Still on market
France		Still on market

Device identification

Trade name: System with "Venturi" type ejectors in the terminal units
UDI-DI code: 08057592370129
Basic UDI-DI: 805759237MAGSSJG
Reference / catalog number: System with "Venturi" type ejectors in the terminal units
Issuing entity: GS1

Classification

Risk category: Class IIa
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: 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)08057592370129

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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.

Z120309MEDICAL/MEDICINAL GAS PIPELINE SYSTEMS AND RELATED ACCESSORIES

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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