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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

MDARGB50 — Class IIa MDD by Acail Gás S.A.

MD Atlas
Acail Gás S.A.

EUDAMED last updated this device on Mar 10, 2026

MDARGB50

B-05600731257114

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Acail Gás S.A.
UDI-DI code: 05600731257114
Reference / catalog number: MDARGB50

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View device family (Basic UDI)

Manufacturer information

Organization name: Acail Gás S.A.
SRN: PT-MF-000007103
Manufacturer status: Active

Related devices

MDCO2B03B-05600731257008On the market MDCO2B07B-05600731257046On the market MDARGB07B-05600731257091On the market MDCO2B07PINB-05600731257053On the market MDARGB05B-05600731257084On 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

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

CW268
Contem gás sob pressão: risco de explosão sob a ação do calor.

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Market distribution

Primary placement in Portugal; available across 1 country total.

Country	On market since	Until
PortugalPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05600731257114
Basic UDI-DI: B-05600731257114
Reference / catalog number: MDARGB50
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: Argon for cryosurgery and electrosurgery, packaged in cylinders.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 50 MU34

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05600731257114

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

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

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