Taiwan FDA registration 236a79b58426ad08e9ae425d460f05df
“Kirwan” Reusable Bipolar Forceps
TW: “柯恩”可重複使用雙極電燒鑷子
Taiwan·Risk Class 2·MD·KIRWAN SURGICAL PRODUCTS, LLC.·Registered Mar 23, 2018 – Mar 23, 2028ActiveRegistration details
- Analysis ID
- 236a79b58426ad08e9ae425d460f05df
- License Form
- Ministry of Health Medical Device Import No. 030997
- Customs Code
- DHA05603099709
Company information
- Manufacturer
- KIRWAN SURGICAL PRODUCTS, LLC.
- Manufacturer Country
- United States
- Authorized Representative
- AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4400 Electric knife for cutting and hemostasis and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 23, 2018
- Expiry Date
- Mar 23, 2028
About this record
Access comprehensive regulatory information for “Kirwan” Reusable Bipolar Forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 236a79b58426ad08e9ae425d460f05df and manufactured by KIRWAN SURGICAL PRODUCTS, LLC.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).
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