Pure Global AI
EUDAMED registration B140BM55940No

Airflow Cannula

BRAEBON Medical CorporationClass IEU EUDAMEDTrade name: Divided Nasal Cannula
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
Z12100585
Trade name
Divided Nasal Cannula
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
B140BM55940
Basic UDI
++B140CannulaPD
Version date
July 12, 2024
Manufacturer last update
March 17, 2021
Active status
No
Manufacturer
Manufacturer name
BRAEBON Medical Corporation
Country
Canada
Country type
NON_EU
Address
100 Schneider Road Kanata
Email
info@braebon.com
Authorized representative
Name
CEpartner4U
SRN
NL-AR-000000111
Country
Netherlands
Address
13 Esdoornlaan Maarn
Email
office@cepartner4u.com
Telephone
+31343442524
Regulatory information
Competent authority
Ministerie van Volksgezondheid, Welzijn en Sport
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
France
Market available
France:None~None, Germany:None~None, Italy:None~None, Portugal:None~None, Spain:None~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

POLYSOMNOGRAPHY INSTRUMENTS - CONSUMABLES

About this record

Access comprehensive regulatory information for Airflow Cannula in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI B140BM55940 and manufactured by BRAEBON Medical Corporation in Canada.

This page provides complete registration details including trade name (Divided Nasal Cannula), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.