Taiwan FDA registration 11d225d10f2870e468f4539e47889e65
"Swiss Bo" reinhalation device (unsterilized)
TW: "瑞士博" 再吸入裝置(未滅菌)
Taiwan·Risk Class 1·RESPIRONICS, INC.·Registered Apr 25, 2006 – Apr 25, 2016CancelledRegistration details
- Analysis ID
- 11d225d10f2870e468f4539e47889e65
- Customs Code
- DHA04400421600
Company information
- Manufacturer
- RESPIRONICS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BROJAW INC.
Product details
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5675 Re-inhalation device
- Import Information
- import
Dates and status
- Registration Date
- Apr 25, 2006
- Expiry Date
- Apr 25, 2016
- Cancellation Date
- May 17, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Swiss Bo" reinhalation 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 11d225d10f2870e468f4539e47889e65 and manufactured by RESPIRONICS, INC.. The authorized representative in Taiwan is BROJAW INC..
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