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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

KB040024 — Class IIb MDR by Air Liquide Medical…

MD Atlas
Air Liquide Medical Systems S.A.

EUDAMED last updated this device on Jan 13, 2025

KB040024

37005043MONNALTEO9H

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: 03700504302200
Reference / catalog number: KB040024

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Manufacturer information

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

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
-

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: 03700504302200
Basic UDI-DI: 37005043MONNALTEO9H
Reference / catalog number: KB040024
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z1203010504ADULT AND PAEDIATRIC/NEONATAL PULMONARY VENTILATORS

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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