Taiwan FDA registration da6a649f40e607b0771a2e1846e42949
"General Medicine" Rigid Laryngoscopy (Unsterilized)
TW: "普醫" 硬式喉頭鏡 (未滅菌)
Taiwan·Risk Class 1·PROACT MEDICAL LTD.·Registered Oct 08, 2010 – Oct 08, 2015CancelledRegistration details
- Analysis ID
- da6a649f40e607b0771a2e1846e42949
- Customs Code
- DHA04400933300
Company information
- Manufacturer
- PROACT MEDICAL LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- PHOENIX INSTRUMENT BUSINESS CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Rigid Laryngoscopy (D.5540)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5540 Rigid laryngoscope
- Import Information
- import
Dates and status
- Registration Date
- Oct 08, 2010
- Expiry Date
- Oct 08, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "General Medicine" Rigid Laryngoscopy (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number da6a649f40e607b0771a2e1846e42949 and manufactured by PROACT MEDICAL LTD.. The authorized representative in Taiwan is PHOENIX INSTRUMENT BUSINESS CO., LTD..
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