Taiwan FDA registration 512f4f3f57ad759ea114b590abc8b667
Prylmosyot II fully automated autoclave liquid chromatography (unsterilized)
TW: 普林莫斯優特二型全自動化高壓液相層析儀（未滅菌）
Taiwan·Risk Class 1·Trinity Biotech (Primus Corporation dba Trinity Biotech)·Registered Mar 24, 2006 – Mar 24, 2026CancelledRegistration details
- Analysis ID
- 512f4f3f57ad759ea114b590abc8b667
- Customs Code
- DHA04400315205
Company information
- Manufacturer Country
- United States
- Authorized Representative
- PROGRESSIVE GROUP INC.
Product details
- Intended Use
- A device that separates one or more drugs or compounds from a solution.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2260 High-pressure liquid chromatography for clinical use
- Import Information
- import
Dates and status
- Registration Date
- Mar 24, 2006
- Expiry Date
- Mar 24, 2026
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for Prylmosyot II fully automated autoclave liquid chromatography (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 512f4f3f57ad759ea114b590abc8b667 and manufactured by Trinity Biotech (Primus Corporation dba Trinity Biotech). The authorized representative in Taiwan is PROGRESSIVE GROUP INC..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices