Taiwan FDA registration 0d030c1941e53380f3e37ef6cce88d6b
“QIAGEN” RNeasy DSP FFPE Kit
TW: “凱杰” 福馬林固定石蠟包埋樣品RNA純化試劑組
Taiwan·Risk Class 2·MD·QIAGEN GMBH·Registered Jun 22, 2020 – Jun 22, 2025ExpiredRegistration details
- Analysis ID
- 0d030c1941e53380f3e37ef6cce88d6b
- License Form
- Ministry of Health Medical Device Import No. 033494
- Customs Code
- DHA05603349401
Company information
- Manufacturer
- QIAGEN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- QIAGEN TAIWAN COMPANY LIMITED
Product details
- Intended Use
- This product is used to purify total RNA from formalin-fixed (paraffin embeddedded, FFPE) treated tissues.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C4070 Ribonucleic acid analysis pretreatment system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 22, 2020
- Expiry Date
- Jun 22, 2025
About this record
Access comprehensive regulatory information for “QIAGEN” RNeasy DSP FFPE Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0d030c1941e53380f3e37ef6cce88d6b and manufactured by 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