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Organization name
UDI-DI code
Reference / catalog number

008830 — Class IIa MDR by Nippon Sanso…

MD Atlas
Nippon Sanso Deutschland GmbH

EUDAMED last updated this device on Mar 13, 2025

008830

426021581CO2MEDV8

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Nippon Sanso Deutschland GmbH
UDI-DI code: 04260215811068
Reference / catalog number: 008830

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Manufacturer information

Organization name: Nippon Sanso Deutschland GmbH
SRN: DE-MF-000005116
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

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

CW010
EUDAMED did not publish a description for this code.
CW007
Vor der ersten Benutzung muss der Druckgasbehälter mit einem intakten Originalitätsverschluss versehen sein.
CW032
EUDAMED did not publish a description for this code.
CW132
EUDAMED did not publish a description for this code.
CW040
EUDAMED did not publish a description for this code.
CW071
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	Jan 1, 2010	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260215811068
Basic UDI-DI: 426021581CO2MEDV8
Reference / catalog number: 008830
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: 10 Liter = 7,5 Kg
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

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Expiration date
Manufacturing date
Serial number
Software identification