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Posterior Lumbar Interbody Fusion System CanPEEK-P Instrument Set Newer version - ARCSA Registration b1cc0396050c306631bb879f23ed1208

Access comprehensive regulatory information for Posterior Lumbar Interbody Fusion System CanPEEK-P Instrument Set Newer version in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID b1cc0396050c306631bb879f23ed1208 and manufactured by CANWELL MEDICAL CO., LTD. The device was registered on June 20, 2023.

This page provides complete registration details including 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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I
b1cc0396050c306631bb879f23ed1208
Posterior Lumbar Interbody Fusion System CanPEEK-P Instrument Set Newer version
ARCSA ID: b1cc0396050c306631bb879f23ed1208
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Device Classification
Risk Class
I
Registration Information
Analysis ID
b1cc0396050c306631bb879f23ed1208
Registration Date
June 20, 2023
Expiration Date
June 20, 2028
Manufacturer
Country
CHINA
Authorized Representative
Phone
43884072