Taiwan FDA registration e61eaff3143c00932b99089b5e7d8ffa
"CareFusion" Surgical Clipper(Non-sterile)
TW: "卡福"外科除毛器(未滅菌)
Taiwan·Risk Class 1·MD·CAREFUSION CORPORATION·Registered Jun 19, 2014 – Jun 19, 2019CancelledRegistration details
- Analysis ID
- e61eaff3143c00932b99089b5e7d8ffa
- License Form
- Ministry of Health Medical Device Import No. 014266
- Customs Code
- DHA09401426601
Company information
- Manufacturer
- CAREFUSION CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- MEDITECHS INSTRUMENTS CO., LTD.
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 19, 2014
- Expiry Date
- Jun 19, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "CareFusion" Surgical Clipper(Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e61eaff3143c00932b99089b5e7d8ffa and manufactured by CAREFUSION CORPORATION. The authorized representative in Taiwan is MEDITECHS INSTRUMENTS CO., LTD..
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