Taiwan FDA registration 67cf5176db619820e4199877da9e8b23
"Tesco" tracheal dilator forceps (unsterilized)
TW: “泰斯科”氣管擴張鉗 (未滅菌)
Taiwan·Risk Class 1·TIMESCO OF LONDON LTD.,·Registered Nov 04, 2011 – Nov 04, 2016CancelledRegistration details
- Analysis ID
- 67cf5176db619820e4199877da9e8b23
- Customs Code
- DHA04401101708
Company information
- Manufacturer
- TIMESCO OF LONDON LTD.,
- Manufacturer Country
- United Kingdom
- Authorized Representative
- CEMMA MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "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
- import
Dates and status
- Registration Date
- Nov 04, 2011
- Expiry Date
- Nov 04, 2016
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Tesco" tracheal dilator forceps (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 67cf5176db619820e4199877da9e8b23 and manufactured by TIMESCO OF LONDON LTD.,. The authorized representative in Taiwan is CEMMA MEDICAL CO., LTD..
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