Taiwan FDA registration 44e484cd3e3005113e94618542dee9be
"Swiss Bo" suction aid (unsterilized)
TW: "瑞士博"吸藥輔助器(未滅菌)
Taiwan·Risk Class 1·RESPIRONICS, INC.·Registered Apr 14, 2006 – Apr 14, 2016CancelledRegistration details
- Analysis ID
- 44e484cd3e3005113e94618542dee9be
- Customs Code
- DHA04400392702
Company information
- Manufacturer
- RESPIRONICS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BROJAW INC.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-respiratory Medical Aerosol Device (D.5640)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5640 非呼吸用醫藥噴霧器(atomizer)
- Import Information
- import
Dates and status
- Registration Date
- Apr 14, 2006
- Expiry Date
- Apr 14, 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" suction aid (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 44e484cd3e3005113e94618542dee9be and manufactured by RESPIRONICS, INC.. The authorized representative in Taiwan is BROJAW INC..
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