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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

CO2 Médical pour endoscopie — Class IIa MDD by Messer France

MD Atlas
Messer France

EUDAMED last updated this device on Oct 4, 2022

CO2 Médical pour endoscopie

B-03770021031006

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Messer France
UDI-DI code: 03770021031006
Reference / catalog number: 103027027

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Manufacturer information

Organization name: Messer France
SRN: FR-MF-000013256
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: CO2 Médical pour endoscopie
UDI-DI code: 03770021031006
Basic UDI-DI: B-03770021031006
Reference / catalog number: 103027027
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: La cœlioscopie consiste à accéder à la cavité abdominale sans ouvrir la paroi abdominale. Du gaz carbonique (CO2) est introduit dans la cavité abdominale. La pression positive exercée par ce gaz va soulever la paroi abdominale, créant ainsi un espace entre la paroi et les viscères où le chirurgien peut regarder et où il peut introduire ses instruments pour opérer.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0901CLINICAL/THERAPEUTIC APPLICATIONS CARBON DIOXIDE

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

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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.