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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

SDGM-SODIGIS — Class IIb MDR by SODIGIS

MD Atlas
SODIGIS

EUDAMED last updated this device on May 5, 2022

SDGM-SODIGIS

3770021702SDGMWB

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SODIGIS
UDI-DI code: 03770021702074
Reference / catalog number: SDGM-SODIGIS

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Manufacturer information

Organization name: SODIGIS
SRN: FR-MF-000004177
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	May 5, 2022	Dec 31, 2050

Device identification

Trade name: SDGM-SODIGIS
UDI-DI code: 03770021702074
Basic UDI-DI: 3770021702SDGMWB
Reference / catalog number: SDGM-SODIGIS
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: SYSTEME DE DISTRIBUTION DE GAZ MEDICAUX
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

This device is not currently linked to any other device.

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.