Taiwan FDA registration fe66593ca91b5a3b5ca79667b4f1c1a0
"Speed" closed suction device (unsterilized)
TW: "飛速" 密閉式吸痰器 (未滅菌)
Taiwan·Risk Class 1·AOK TOOLING LTD·Registered Jul 27, 2015 – Jul 27, 2020CancelledRegistration details
- Analysis ID
- fe66593ca91b5a3b5ca79667b4f1c1a0
- Customs Code
- DHA09600246007
Company information
- Manufacturer
- AOK TOOLING LTD
- Manufacturer Country
- China
- Authorized Representative
- AOK MEDTECH INC.
Product details
- Intended Use
- Limited to the management method of medical equipment, tracheobronchial suction catheter (D.6810) level 1 identification range.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.6810 Pneumatic bronchial suction guide tube
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jul 27, 2015
- Expiry Date
- Jul 27, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Speed" closed suction device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fe66593ca91b5a3b5ca79667b4f1c1a0 and manufactured by AOK TOOLING LTD. The authorized representative in Taiwan is AOK MEDTECH INC..
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