Taiwan FDA registration 5c3aa08e44aab9335cb3fab55635ef41
Tekken Sunrise Analyzer (Unsterilized)
TW: 提肯日出分析儀 (未滅菌)
Taiwan·Risk Class 1·TECAN SCHWEIZ AG·Registered Nov 08, 2006 – Nov 08, 2016CancelledRegistration details
- Analysis ID
- 5c3aa08e44aab9335cb3fab55635ef41
- Customs Code
- DHA04400531402
Company information
- Manufacturer
- TECAN SCHWEIZ AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- 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
- import
Dates and status
- Registration Date
- Nov 08, 2006
- Expiry Date
- Nov 08, 2016
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Tekken Sunrise Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5c3aa08e44aab9335cb3fab55635ef41 and manufactured by TECAN SCHWEIZ AG. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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