Taiwan FDA registration ca93d3938f868a167639adbfc70f47ab
Grifols Triturus Analyzer(non-sterile)
TW: 葛林弗全自動酵素免疫分析儀(未滅菌)
Registration details
- Analysis ID
- ca93d3938f868a167639adbfc70f47ab
- License Form
- Ministry of Health Medical Device Import Registration No. 005264
- Customs Code
- DHA08400526400
Company information
- Manufacturer
- DIAGNOSTIC GRIFOLS S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2500 Enzyme Analyzer for Clinical Use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Grifols Triturus Analyzer(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 ca93d3938f868a167639adbfc70f47ab and manufactured by DIAGNOSTIC GRIFOLS S.A.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) 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.
Free DatabasePowered by Pure Global AI89,000+ Devices