"PRF" Automated Sedimentation Rate Device (Non-Sterile) - Taiwan Registration 223d1aaf9446c6544f9b896bee7db7bd
Access comprehensive regulatory information for "PRF" Automated Sedimentation Rate Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 223d1aaf9446c6544f9b896bee7db7bd and manufactured by SARL PROCESS FOR PRF. The authorized representative in Taiwan is ADENT MED CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including SARL PROCESS FOR PRF, PROCESS FOR PRF S.A.R.L, and 4 recent registrations in the same category. 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
223d1aaf9446c6544f9b896bee7db7bd
Ministry of Health Medical Device Import No. 016247
DHA09401624704
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Automatic Sedimentation Rate Device (B.5800)".
B Hematology and pathology devices
B5800 Automatic Settling Rate Device
Imported from abroad
Dates and Status
Mar 11, 2016
Mar 11, 2021
"PRF" Automated Sedimentation Rate Device (Non-Sterile)
SARL PROCESS FOR PRF
470e8c10f5360c3f7b2850acd158e071
1
"PRF" Automated sedimentation rate device (NON-STERILE)
PROCESS FOR PRF S.A.R.L
70849deac162543c35a4dc3373231374
1
"PRF" Automated Sedimentation Rate Device (Non-Sterile)
SARL PROCESS FOR PRF
3bc66fb2146d29cc3bc4284a8e409129
1
"PRF" Automated sedimentation rate device (NON-STERILE)
PROCESS FOR PRF S.A.R.L
dd393b178e9a5b30895529bdf4d006ac
1

