7023374NP DIACAN PRO - ARCSA Registration d9aabbd57545ad26a9541eff97d6ff6a
Access comprehensive regulatory information for 7023374NP DIACAN PRO in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID d9aabbd57545ad26a9541eff97d6ff6a and manufactured by NIPRO (THAILAND) CORPORATION LIMITED. The device was registered on August 24, 2017.
This page provides complete registration details including product type (Invasive), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.
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ARCSA Official Data
II
d9aabbd57545ad26a9541eff97d6ff6a
7023374NP DIACAN PRO
ARCSA ID: d9aabbd57545ad26a9541eff97d6ff6a
Device Classification
Risk Class
II
Product Type
Invasive
Brand Name
DIACAN
Commercial Name
Needles, for Hemodialysis, Arterio-Venous Fistula
Registration Information
Analysis ID
d9aabbd57545ad26a9541eff97d6ff6a
Registration Date
August 24, 2017
Expiration Date
August 24, 2027
Product Use
DISPOSABLE VASCULAR ACCESS FISTULA NEEDLE FOR EXTRACORPOREAL THERAPIES.
Manufacturer
City
PHRA NAKHON
Country
THAILAND
Address
10/2 MOO 8 BANGNOMKO, SENA, PHRA NAKHON SI AYUTTHAYA13110
Product Owner
Name
B. BRAUN AVITUM AG
Country
GERMANY
Authorized Representative