Taiwan FDA registration c19792d8d087a2ed8b1ce667708161c0
"Ambar" electronic bronchoscope and screen
TW: “安寶”電子式支氣管鏡及螢幕
Taiwan·Risk Class 2·AMBU SDN BHD;; AMBU A/S·Registered Jan 30, 2015 – Jan 30, 2020CancelledRegistration details
- Analysis ID
- c19792d8d087a2ed8b1ce667708161c0
- Customs Code
- DHA05602697408
Company information
- Manufacturer
- AMBU SDN BHD;; AMBU A/S
- Manufacturer Country
- Malaysia;;Denmark
- Authorized Representative
- CHINA SPRING TRADING CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4680 Bronchial tubescopes (soft or rigid) and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- Jan 30, 2015
- Expiry Date
- Jan 30, 2020
- 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 "Ambar" electronic bronchoscope and screen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c19792d8d087a2ed8b1ce667708161c0 and manufactured by AMBU SDN BHD;; AMBU A/S. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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