Taiwan FDA registration c57f6eefc149b6b62f69ec6fc2911a1a
"Jingleng" inner tracheal tube
TW: "京冷"氣管內管
Taiwan·HANGZHOU JINLIN MEDICAL APPLIANCES CO., LTD·Registered May 02, 2006 – May 02, 2011CancelledRegistration details
- Analysis ID
- c57f6eefc149b6b62f69ec6fc2911a1a
- Customs Code
- DHA04200010902
Company information
- Manufacturer
- HANGZHOU JINLIN MEDICAL APPLIANCES CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- Daihatsu Medical Equipment Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- May 02, 2006
- Expiry Date
- May 02, 2011
- Cancellation Date
- Jan 17, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Jingleng" inner tracheal tube in Taiwan's medical device market through Pure Global AI's free database. is registered under number c57f6eefc149b6b62f69ec6fc2911a1a and manufactured by HANGZHOU JINLIN MEDICAL APPLIANCES CO., LTD. The authorized representative in Taiwan is Daihatsu Medical Equipment Co., 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