Taiwan FDA registration b1fb43e68b7c35714cca2ba45ca68d2c
Proway Instrument Guide Series (Sterilization)
TW: "普威"器械引導器系列(滅菌)
Taiwan·Risk Class 1·Proway International Limited·Registered Apr 12, 2006 – Apr 12, 2021CancelledRegistration details
- Analysis ID
- b1fb43e68b7c35714cca2ba45ca68d2c
- Customs Code
- DHY04300118506
Company information
- Manufacturer
- Proway International Limited
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Proway International Limited
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment (Manual Instruments for General Surgery [I.4800]).
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Apr 12, 2006
- Expiry Date
- Apr 12, 2021
- Cancellation Date
- Sep 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Proway Instrument Guide Series (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b1fb43e68b7c35714cca2ba45ca68d2c and manufactured by Proway International Limited. The authorized representative in Taiwan is Proway International Limited.
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