Taiwan FDA registration 65f99ab20fa4d21488dae4e1035a85f3
"Pumei" electric plaster removal device (unsterilized)
TW: "普美" 電動石膏拆除器械 (未滅菌)
Taiwan·Risk Class 1·PRO-MED INSTRUMENTE GMBH·Registered Feb 20, 2006 – Feb 20, 2011CancelledRegistration details
- Analysis ID
- 65f99ab20fa4d21488dae4e1035a85f3
- Customs Code
- DHA04400264306
Company information
- Manufacturer
- PRO-MED INSTRUMENTE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- WONDERFUL INSTRUMENTS COMPANY, LTD.
Product details
- Intended Use
- A cast removal device is an alternating current, hand-held device that removes a patient's cast.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.5960 石膏拆除器械
- Import Information
- import
Dates and status
- Registration Date
- Feb 20, 2006
- Expiry Date
- Feb 20, 2011
- Cancellation Date
- Jan 18, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Pumei" electric plaster removal 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 65f99ab20fa4d21488dae4e1035a85f3 and manufactured by PRO-MED INSTRUMENTE GMBH. The authorized representative in Taiwan is WONDERFUL INSTRUMENTS COMPANY, LTD..
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