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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

IVF — Class IIa MDD by S.E. Carburos…

MD Atlas
S.E. Carburos Metálicos, S.A.

EUDAMED last updated this device on Sep 23, 2022

IVF

B-08420219100056

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: S.E. Carburos Metálicos, S.A.
UDI-DI code: 08420219100056
Reference / catalog number: IVF

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Manufacturer information

Organization name: S.E. Carburos Metálicos, S.A.
SRN: ES-MF-000003117
Manufacturer status: Active

Critical warnings

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

CW203
En caso de fuga en un ambiente confinado puede haber riesgo de asfixia a altas concentraciones.
CW184
En caso de fuga en un ambiente confinado puede haber riesgo de asfixia a altas concentraciones.
CW132
Para más información consulte la ficha de datos de seguridad.
CW086
No inhalar.

Market distribution

Primary placement in Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement	Sep 22, 2010	Still on market
Portugal	Jun 28, 2018	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08420219100056
Basic UDI-DI: B-08420219100056
Reference / catalog number: IVF
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: Misturas de CO2/O2/N2. Cilindro de gás de alumínio ou aço com válvula de conexão padronizada.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12080299GYNAECOLOGY AND FERTILITY TREATMENT INSTRUMENTS - OTHER

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

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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.