Taiwan FDA registration f046b22e7b8344df65de60c442fb2e99
“BIOLATEX” Lp(a) Reagent Kit (Non-Sterile)
TW: “醫信”脂蛋白(a)檢驗試劑組(未滅菌)
Taiwan·Risk Class 1·MD·BIOLATEX·Registered Jan 14, 2021 – Jan 14, 2026ExpiredRegistration details
- Analysis ID
- f046b22e7b8344df65de60c442fb2e99
- License Form
- Ministry of Health Medical Device Import No. 022246
- Customs Code
- DHA09402224601
Company information
- Manufacturer
- BIOLATEX
- Manufacturer Country
- Spain
- Authorized Representative
- HONEST MEDICAL INC.
Product details
- Intended Use
- Limited to the first level recognition range of the lipoprotein test system (A.1475) of the medical device management method.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1475 Lipoprotein Testing System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 14, 2021
- Expiry Date
- Jan 14, 2026
About this record
Access comprehensive regulatory information for “BIOLATEX” Lp(a) Reagent Kit (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 f046b22e7b8344df65de60c442fb2e99 and manufactured by BIOLATEX. The authorized representative in Taiwan is HONEST MEDICAL 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