Taiwan FDA registration 2de6d8788323984df1abaa234c7065e0
"Camelman" throat mask (unsterilized)
TW: “駝人”喉頭面罩 (未滅菌)
Taiwan·Risk Class 1·XINXIANG CITY TUOREN MEDICAL DEVICE CO., LTD.·Registered Jan 22, 2014 – Jan 22, 2019CancelledRegistration details
- Analysis ID
- 2de6d8788323984df1abaa234c7065e0
- Customs Code
- DHA09600205906
Company information
- Manufacturer
- XINXIANG CITY TUOREN MEDICAL DEVICE CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- ELC ENTERPRISE LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5110 Oropharyngeal airway tubes
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jan 22, 2014
- Expiry Date
- Jan 22, 2019
- 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 "Camelman" throat mask (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2de6d8788323984df1abaa234c7065e0 and manufactured by XINXIANG CITY TUOREN MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is ELC ENTERPRISE LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices