Taiwan FDA registration e1340ad1659cb6afdc341879e83b61e8
"Kaijie" microtitration dilution and dispensing equipment (unsterilized)
TW: "凱杰" 微滴定稀釋及分配器材(未滅菌)
Taiwan·Risk Class 1·QIAGEN GMBH·Registered Jul 23, 2012 – Jul 23, 2022CancelledRegistration details
- Analysis ID
- e1340ad1659cb6afdc341879e83b61e8
- Customs Code
- DHA04401197506
Company information
- Manufacturer
- QIAGEN GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- QIAGEN TAIWAN COMPANY LIMITED
Product details
- Intended Use
- Limited to the first level identification range of microtitration dilution and dispensing equipment (C.2500) of the management measures for medical devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2500 微滴定稀釋及分配器材
- Import Information
- import
Dates and status
- Registration Date
- Jul 23, 2012
- Expiry Date
- Jul 23, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kaijie" microtitration dilution and dispensing equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e1340ad1659cb6afdc341879e83b61e8 and manufactured by QIAGEN GMBH. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.
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