Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

AO.20.04 — 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.20.04

B-03760349880035

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: GAZ MEDICAUX DE L'OUEST
UDI-DI code: 03760349880035
Reference / catalog number: AO.20.04

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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.20.08B-03760349880059On the market AO.20.09B-03760349880066On the market AO.21.01B-03760349880080On 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	Feb 3, 2023	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03760349880035
Basic UDI-DI: B-03760349880035
Reference / catalog number: AO.20.04
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: CHBA JOSSELIN "Restructuration du 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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification