Taiwan FDA registration f2d38fc809f4041563d800912fa6cd6c
"Mintec" liquid drug applicator (unsterilized)
TW: “明泰科”液體藥物給藥器(未滅菌)
Taiwan·Risk Class 1·MINNTECH CORPORATION·Registered Aug 31, 2007 – Aug 31, 2017CancelledRegistration details
- Analysis ID
- f2d38fc809f4041563d800912fa6cd6c
- Customs Code
- DHA04400611807
Company information
- Manufacturer
- MINNTECH CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Huizhong Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Liquid Drug Dispenser (J.6430)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6430 液體藥物給藥器
- Import Information
- import
Dates and status
- Registration Date
- Aug 31, 2007
- Expiry Date
- Aug 31, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Mintec" liquid drug applicator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f2d38fc809f4041563d800912fa6cd6c and manufactured by MINNTECH CORPORATION. The authorized representative in Taiwan is Huizhong Co., Ltd.
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