Taiwan FDA registration 1623b0396a72bc71ea8bd0fd4f247392
"Daiichi" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile)
TW: "大壹器" 耳鼻喉光纖光源及載具 (未滅菌)
Taiwan·Risk Class 1·MD·DAIICHI MEDICAL CO., LTD.·Registered Aug 05, 2013 – Aug 05, 2028ActiveRegistration details
- Analysis ID
- 1623b0396a72bc71ea8bd0fd4f247392
- License Form
- Ministry of Health Medical Device Import No. 013276
- Customs Code
- DHA09401327609
Company information
- Manufacturer
- DAIICHI MEDICAL CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- GIA HO INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4350 ENT fiber optic light source and vehicle
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 05, 2013
- Expiry Date
- Aug 05, 2028
About this record
Access comprehensive regulatory information for "Daiichi" Ear, nose, and throat fiberoptic light source and carrier (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 1623b0396a72bc71ea8bd0fd4f247392 and manufactured by DAIICHI MEDICAL CO., LTD.. The authorized representative in Taiwan is GIA HO INSTRUMENTS CO., LTD..
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