Taiwan FDA registration 60bff896a8ff200e0dffcd55587d8254
"Kaijie" Yili automatic nucleic acid purification system (unsterilized)
TW: "凱杰" 伊利全自動核酸純化系統 (未滅菌)
Taiwan·Risk Class 1·Plexus Manufacturing Sdn. Bhd.;; QIAGEN GMBH·Registered Aug 01, 2023 – Aug 01, 2028ActiveRegistration details
- Analysis ID
- 60bff896a8ff200e0dffcd55587d8254
- Customs Code
- DHA09402319209
Company information
- Manufacturer
- Plexus Manufacturing Sdn. Bhd.;; QIAGEN GMBH
- Manufacturer Country
- Malaysia;;Germany
- Authorized Representative
- QIAGEN TAIWAN COMPANY LIMITED
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, the first level identification range of the "ribonucleonic acid analysis pretreatment system (C.4070)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.4070 核醣核酸分析前處理系統
- Import Information
- 輸入;; 委託製造;; QMS/QSD
Dates and status
- Registration Date
- Aug 01, 2023
- Expiry Date
- Aug 01, 2028
About this record
Access comprehensive regulatory information for "Kaijie" Yili automatic nucleic acid purification system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 60bff896a8ff200e0dffcd55587d8254 and manufactured by Plexus Manufacturing Sdn. Bhd.;; QIAGEN GMBH. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.
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