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Organization name
UDI-DI code
Reference / catalog number

Unit of use 1 Liter — Class IIa MDR by Nippon Sanso…

MD Atlas
Nippon Sanso Deutschland GmbH

EUDAMED last updated this device on Mar 13, 2025

Unit of use 1 Liter

426021581CO2MEDV8

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Nippon Sanso Deutschland GmbH
UDI-DI code: 04260215811020
Reference / catalog number: Unit of use 1 Liter

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Manufacturer information

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

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: 04260215811020
Basic UDI-DI: 426021581CO2MEDV8
Reference / catalog number: Unit of use 1 Liter
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: Die "Unit of Use 1 Liter" ist selbst kein Medizinprodukt, sondern nur eine Basisinformation für die Produktfamilie "Medizinisches Kohlendioxid".
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

Related devices

006830426021581CO2MEDV8On the market 002830426021581CO2MEDV8On the market 001830426021581CO2MEDV8On the market 030830426021581CO2MEDV8On the market 010830426021581CO2MEDV8On 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.