"Kaijie" cold light meter (unsterilized)
Taiwan·Risk Class 1·QIAGEN GMBH·Registered Sep 14, 2012 – Sep 14, 2017Cancelled- Analysis ID
- 75149c9af9075b041e35441317eca0b5
- Customs Code
- DHA04401216604
- Manufacturer
- QIAGEN GMBH
- Manufacturer Country
- Germany
- 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
- Sep 14, 2012
- Expiry Date
- Sep 14, 2017
- Cancellation Date
- Nov 20, 2019
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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 75149c9af9075b041e35441317eca0b5 and manufactured by QIAGEN GMBH. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including QIAGEN, QIAGEN GAITHERSBURG, INC., 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.