Taiwan FDA registration fe75a92ddc3197fc364d851834eba1dd
"Speth" Beston anesthetic volatilizer
TW: “斯貝司”百利得通麻醉藥揮發器
Taiwan·Risk Class 2·Spacelabs Healthcare Medical Equipment(Suzhou) Co., Ltd.·Registered Jan 06, 2015 – Jan 06, 2020CancelledRegistration details
- Analysis ID
- fe75a92ddc3197fc364d851834eba1dd
- Customs Code
- DHA09200064302
Company information
- Manufacturer Country
- China
- Authorized Representative
- CHARITY 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.5880 Anesthetic drug transmitter
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jan 06, 2015
- Expiry Date
- Jan 06, 2020
- Cancellation Date
- Sep 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Speth" Beston anesthetic volatilizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fe75a92ddc3197fc364d851834eba1dd and manufactured by Spacelabs Healthcare Medical Equipment(Suzhou) Co., Ltd.. The authorized representative in Taiwan is CHARITY PHARMACEUTICAL CO., LTD..
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