"Kaijie" automatic capillary electrophoresis instrument (unsterilized)
Taiwan·Risk Class 1·QIAGEN GMBH·Registered Dec 07, 2012 – Dec 07, 2017Cancelled- Analysis ID
- cc4556742d8d64df719126ebfdc9f734
- Customs Code
- DHA04401245103
- Manufacturer
- QIAGEN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- QIAGEN TAIWAN COMPANY LIMITED
- Intended Use
- Limited to the first level identification scope of "Electrophoresis Equipment for Clinical Use (A.2485)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2485 Electrophoresis equipment for clinical use
- Import Information
- Input;; QMS/QSD
- Registration Date
- Dec 07, 2012
- Expiry Date
- Dec 07, 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" 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 cc4556742d8d64df719126ebfdc9f734 and manufactured by QIAGEN 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;; Zollner Electronics 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.