Taiwan FDA registration 1c4bcd9e6bf50922534cf16ec906cd84
"Aerox" respirator
TW: “艾羅克斯”呼吸器
Taiwan·Risk Class 2·AIROX·Registered Dec 18, 2008 – Dec 18, 2013CancelledRegistration details
- Analysis ID
- 1c4bcd9e6bf50922534cf16ec906cd84
- Customs Code
- DHA00601950900
Company information
- Manufacturer
- AIROX
- Manufacturer Country
- France
- Authorized Representative
- Taiwan Tyco Pharmaceutical Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5905 Non-continuous respirators
- Import Information
- import
Dates and status
- Registration Date
- Dec 18, 2008
- Expiry Date
- Dec 18, 2013
- Cancellation Date
- Apr 23, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Aerox" respirator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c4bcd9e6bf50922534cf16ec906cd84 and manufactured by AIROX. The authorized representative in Taiwan is Taiwan Tyco Pharmaceutical Co., Ltd.
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