Taiwan FDA registration 1d06089714173f2f405bde3836d70705
Abbott M1000 automatic body examination processing system
TW: 亞培m1000全自動檢體處理系統
Taiwan·Risk Class 1·TECAN SCHWEIZ AG·Registered Nov 21, 2006 – Nov 21, 2011CancelledRegistration details
- Analysis ID
- 1d06089714173f2f405bde3836d70705
- Customs Code
- DHA04400536404
Company information
- Manufacturer
- TECAN SCHWEIZ AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- Fully automatic sample processing system, which can extract nucleic acid substances from samples.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Import Information
- import
Dates and status
- Registration Date
- Nov 21, 2006
- Expiry Date
- Nov 21, 2011
- Cancellation Date
- Nov 06, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Abbott M1000 automatic body examination processing system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1d06089714173f2f405bde3836d70705 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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