Taiwan FDA registration ab853721fff270c4894932b52025fecf
“DA CHUNG” Manual Resuscitator Kit and Accessory
TW: “大中”甦醒球組及其零配件
Taiwan·Risk Class 2·MD·DA CHUNG MEDICAL CO., LTD.·Registered Nov 28, 2013 – Nov 28, 2018CancelledRegistration details
- Analysis ID
- ab853721fff270c4894932b52025fecf
- License Form
- Ministry of Health Medical Device Manufacturing No. 004296
Company information
- Manufacturer
- DA CHUNG MEDICAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DA CHUNG MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5915 Manual Emergency Respirator
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 28, 2013
- Expiry Date
- Nov 28, 2018
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “DA CHUNG” Manual Resuscitator Kit and Accessory in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ab853721fff270c4894932b52025fecf and manufactured by DA CHUNG MEDICAL CO., LTD.. The authorized representative in Taiwan is DA CHUNG MEDICAL CO., LTD..
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