"Kaijie" cold light meter (unsterilized)
Taiwan·Risk Class 1·QIAGEN·Registered Jun 16, 2017 – Jun 16, 2022Cancelled- Analysis ID
- c57860afb6c9508d7af8c7f63eb8b5a2
- Customs Code
- DHA09401797401
- Manufacturer
- QIAGEN
- Manufacturer Country
- United States
- Authorized Representative
- QIAGEN TAIWAN COMPANY LIMITED
- Intended Use
- Limited to the first level identification range of "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2300 Colorimeter, photometer, or spectrophotometer for clinical use
- Import Information
- Input;; QMS/QSD
- Registration Date
- Jun 16, 2017
- Expiry Date
- Jun 16, 2022
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Kaijie" cold light meter (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c57860afb6c9508d7af8c7f63eb8b5a2 and manufactured by QIAGEN. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.
This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including QIAGEN, QIAGEN GMBH, and 4 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.