"Kaijie" cold light meter (unsterilized)
Taiwan·Risk Class 1·QIAGEN GAITHERSBURG, INC.·Registered Jul 24, 2012 – Jul 24, 2017Cancelled- Analysis ID
- 5b6a53467d7869c131416d238f7369fb
- Customs Code
- DHA04401197608
- Manufacturer
- QIAGEN GAITHERSBURG, INC.
- 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
- QMS/QSD;; 輸入
- Registration Date
- Jul 24, 2012
- Expiry Date
- Jul 24, 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 5b6a53467d7869c131416d238f7369fb and manufactured by QIAGEN GAITHERSBURG, INC.. 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 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.