Taiwan FDA registration f95399158bd7c70fb0b959866447e246
“KADEN” Video Intubation Flexible Laryngoscope (Non-Sterile)
TW: “卡德”電子影像喉頭鏡 (未滅菌)
Taiwan·Risk Class 1·MD·KADEN INTERNATIONAL LTD.·Registered May 06, 2014 – May 06, 2019CancelledRegistration details
- Analysis ID
- f95399158bd7c70fb0b959866447e246
- License Form
- Ministry of Health Medical Device Import No. 014111
- Customs Code
- DHA09401411108
Company information
- Manufacturer
- KADEN INTERNATIONAL LTD.
- Manufacturer Country
- Hong Kong
- Authorized Representative
- PRO-READY ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5530 Flexible laryngoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 06, 2014
- Expiry Date
- May 06, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for “KADEN” Video Intubation Flexible Laryngoscope (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 f95399158bd7c70fb0b959866447e246 and manufactured by KADEN INTERNATIONAL LTD.. The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., LTD..
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