"Guanya" hynix lumbar intervertebral fusion device - Taiwan Registration d4a5c1962f510bcc4ffef7b9b3312791
Access comprehensive regulatory information for "Guanya" hynix lumbar intervertebral fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d4a5c1962f510bcc4ffef7b9b3312791 and manufactured by A-SPINE Asia Co., Ltd.. The authorized representative in Taiwan is A-SPINE Asia Co., Ltd..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
d4a5c1962f510bcc4ffef7b9b3312791
DHY00500133709
Product Details
For details, it is Chinese approved copy of the imitation order
N Orthopedics
Domestic
Dates and Status
May 03, 2005
May 03, 2020
Jun 07, 2022
Cancellation Information
Logged out
่จฑๅฏ่ญๅทฒ้พๆๆๆ

