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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

101100044 — Class I MDR by Messer France

MD Atlas
Messer France

EUDAMED last updated this device on Mar 1, 2024

101100044

3770021031ARG300JB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Messer France
UDI-DI code: 03770021031150
Reference / catalog number: 101100044

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Manufacturer information

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

Related devices

Argon médical chirurgical - 200 barB-03770021031112On the market Argon médical chirurgical 200 barB-03770021031129On the market Argon Medical Cryochirurgical 300 bar B503770021031ARG300JBOn the market Argon Medical Cryochirurgical 300 bar CV123770021031ARG300JBOn the market Argon Medical Cryochirurgical 300 bar MP43770021031ARG300JBOn 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.

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW011
Riesgo de asfixia a concentraciones elevadas, en caso de fugas en espacios confinados. Nota: Es posible que la víctima no sea consciente de la asfixia
CW010
EUDAMED did not publish a description for this code.
CW071
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 03770021031150
Basic UDI-DI: 3770021031ARG300JB
Reference / catalog number: 101100044
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: El cilindro de argón de 300 bar debe conectarse a un generador de crioablación. Conexión de salida NEVOC
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 300 MU126
50 MU34

EMDN nomenclature code(s)

V0905CLINICAL/THERAPEUTIC APPLICATIONS ARGON

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