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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

AO.20.08 — Class IIb MDD by GAZ MEDICAUX DE L'OUEST

MD Atlas
GAZ MEDICAUX DE L'OUEST

EUDAMED last updated this device on Aug 31, 2023

AO.20.08

B-03760349880059

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: GAZ MEDICAUX DE L'OUEST
UDI-DI code: 03760349880059
Reference / catalog number: AO.20.08

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Manufacturer information

Organization name: GAZ MEDICAUX DE L'OUEST
SRN: FR-MF-000007657
Manufacturer status: Active

Related devices

AO.18.07B-03760349880004On the market AO.20.07B-03760349880790On the market AO.20.09B-03760349880066On the market AO.21.01B-03760349880080On the market AO.21.03B-03760349880103On 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.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Mar 20, 2023	Still on market

Device identification

Trade name: AO.20.08
UDI-DI code: 03760349880059
Basic UDI-DI: B-03760349880059
Reference / catalog number: AO.20.08
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: GUEMENE S/ SCORFF "Construction CH"
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

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Software identification