Eu Mdr Eu Md Class 2b On The Market

OXO 300

This cylinder valve with integrated regulator and integrated residual pressure valve device is design for oxygen therapy. This Ceodeux S.A. Meditec product will regulate the high pressure of the medical oxygen gas cylinder and deliver it to the patient. This PRODUCT is not intended for any other installation or purpose. If the product user has any question regarding this PRODUCT’s proper application or purpose, the product user should call *352 327832-1 or Fax * 352-32.78.32.317. Any non-approved use or application and/or any non-approved modification of the PRODUCT or its use or application may result in a serious accident or personal injury for which CEODEUX S.A will not be responsible. Ceodeux S.A cannot be held responsible for an inappropriate use of the product. The supplier of the final equipment is responsible for the homologation of the system. CEODEUX S.A. cannot be held responsible of the latter’s negligence. Recommendations of CODEUX S.A. do not substitute for the final responsibility of a customer.

Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0

Basic Information

Primary DI
04262455360016
Basic UDI-DI Code
426245536OXOBasic1CM
Reference
122250 V1
Device Types
None provided
Regulation
Eu Mdr
Classification
Eu Md Class 2b
Status
On The Market

Additional Description

Druckgasflasche BMK2-88-300 und Druckregler M742 00002

Medical Purpose

This cylinder valve with integrated regulator and integrated residual pressure valve device is design for oxygen therapy. This Ceodeux S.A. Meditec product will regulate the high pressure of the medical oxygen gas cylinder and deliver it to the patient. This PRODUCT is not intended for any other installation or purpose. If the product user has any question regarding this PRODUCT’s proper application or purpose, the product user should call *352 327832-1 or Fax * 352-32.78.32.317. Any non-approved use or application and/or any non-approved modification of the PRODUCT or its use or application may result in a serious accident or personal injury for which CEODEUX S.A will not be responsible. Ceodeux S.A cannot be held responsible for an inappropriate use of the product. The supplier of the final equipment is responsible for the homologation of the system. CEODEUX S.A. cannot be held responsible of the latter’s negligence. Recommendations of CODEUX S.A. do not substitute for the final responsibility of a customer.

CND Nomenclature Codes

Code Description
R9099 RESPIRATORY AND ANAESTHESIA DEVICES - OTHER

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