"Kaijie" automatic capillary electrophoresis instrument (unsterilized)
Taiwan·Risk Class 1·QIAGEN GMBH;; Zollner Electronics GmbH·Registered Apr 12, 2022 – Oct 31, 2024Expired- Analysis ID
- 485c70af81dfaace2486eb15450e46cf
- Customs Code
- DHA084a0005203
- Manufacturer
- QIAGEN GMBH;; Zollner Electronics GmbH
- Manufacturer Country
- Germany;;Switzerland
- Authorized Representative
- QIAGEN TAIWAN COMPANY LIMITED
- Intended Use
- Limited to the first level identification range of "Electrophoresis Equipment for Clinical Use (A.2485)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2485 Electrophoresis equipment for clinical use
- Registration Date
- Apr 12, 2022
- Expiry Date
- Oct 31, 2024
Top companies providing products similar to ""Kaijie" automatic capillary electrophoresis instrument (unsterilized)"
Recently registered similar products
Access comprehensive regulatory information for "Kaijie" automatic capillary electrophoresis instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 485c70af81dfaace2486eb15450e46cf and manufactured by QIAGEN GMBH;; Zollner Electronics GmbH. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including QIAGEN GMBH, and 1 recent registrations in the same category. 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.