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Organization name
UDI-DI code
Reference / catalog number

CK062554 — Class IIb MDR by Air Liquide Medical…

MD Atlas
Air Liquide Medical Systems S.A.

EUDAMED last updated this device on Jun 19, 2025

CK062554

37005043XO7A

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Air Liquide Medical Systems S.A.
UDI-DI code: 03700504301302
Reference / catalog number: CK062554

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Manufacturer information

Organization name: Air Liquide Medical Systems S.A.
SRN: FR-MF-000003649
Manufacturer status: Active

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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.

Critical warnings

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

CW010
Consult instructions for use

Market distribution

Primary placement in Ireland; available across 2 countries total.

Country	On market since	Until
IrelandPrimary placement		Still on market
XI		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03700504301302
Basic UDI-DI: 37005043XO7A
Reference / catalog number: CK062554
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Valve integrated pressure regulator with a BS type low pressure outlet and a digital pressure gauge.
Additional information URL: https://medicaldevice.airliquide.com/customer-area
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
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Software identification