Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

006830 — Class IIa MDR by Nippon Sanso…

MD Atlas
Nippon Sanso Deutschland GmbH

EUDAMED last updated this device on Mar 13, 2025

006830

426021581CO2MEDV8

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Nippon Sanso Deutschland GmbH
UDI-DI code: 04260215811051
Reference / catalog number: 006830

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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: 04260215811051
Basic UDI-DI: 426021581CO2MEDV8
Reference / catalog number: 006830
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: 8 Liter = 6 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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.

Related devices

002830426021581CO2MEDV8On the market 001830426021581CO2MEDV8On the market 030830426021581CO2MEDV8On the market 010830426021581CO2MEDV8On the market 004830426021581CO2MEDV8On the market