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Organization name
UDI-DI code
Reference / catalog number

103100052 — Class IIa MDD by Messer Industriegase GmbH

MD Atlas
Messer Industriegase GmbH

EUDAMED last updated this device on Mar 13, 2026

103100052

B-04262389120540

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Messer Industriegase GmbH
UDI-DI code: 04262389120540
Reference / catalog number: 103100052

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Manufacturer information

Organization name: Messer Industriegase GmbH
SRN: DE-MF-000016610
Manufacturer status: Active

Critical warnings

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

CW011
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW024
EUDAMED did not publish a description for this code.
CW999
Suffocating in high concentrations
CW040
EUDAMED did not publish a description for this code.
CW071
EUDAMED did not publish a description for this code.
CW132
EUDAMED did not publish a description for this code.
CW169
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04262389120540
Basic UDI-DI: B-04262389120540
Reference / catalog number: 103100052
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: 5 L (3,75 kg), MIGG
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0901CLINICAL/THERAPEUTIC APPLICATIONS CARBON DIOXIDE

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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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.