Taiwan FDA registration 8211476e4f68dba424846a3b7d46032f
Philips Neopap System
TW: 飛利浦尼歐新生兒呼吸器
Taiwan·Risk Class 2·MD·CHILDREN'S MEDICAL VENTURES·Registered Jan 17, 2014 – Jan 17, 2019CancelledRegistration details
- Analysis ID
- 8211476e4f68dba424846a3b7d46032f
- License Form
- Ministry of Health Medical Device Import No. 025795
- Customs Code
- DHA05602579503
Company information
- Manufacturer
- CHILDREN'S MEDICAL VENTURES
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5905 Discontinuous respirators
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 17, 2014
- Expiry Date
- Jan 17, 2019
- 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 Philips Neopap System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8211476e4f68dba424846a3b7d46032f and manufactured by CHILDREN'S MEDICAL VENTURES. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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