Taiwan FDA registration ecff9d4e5cd93fea479e4042627f6c05
"Lucie" tourniquet (unsterilized)
TW: “路西”止血帶 (未滅菌)
Taiwan·Risk Class 1·WILLY RUSCH GMBH.·Registered Jul 20, 2006 – Jul 20, 2016CancelledRegistration details
- Analysis ID
- ecff9d4e5cd93fea479e4042627f6c05
- Customs Code
- DHA04400494700
Company information
- Manufacturer
- WILLY RUSCH GMBH.
- Manufacturer Country
- Germany
- Authorized Representative
- TRIPLE ROPES ENTERPRISE CO., LTD.
Product details
- Intended Use
- It is limited to the first level of identification of the "Non-inflatable Tourniquet (I.5900)" of the Medical Device Management Regulations.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.5900 非充氣式止血帶
- Import Information
- import
Dates and status
- Registration Date
- Jul 20, 2006
- Expiry Date
- Jul 20, 2016
- Cancellation Date
- Apr 13, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Lucie" tourniquet (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ecff9d4e5cd93fea479e4042627f6c05 and manufactured by WILLY RUSCH GMBH.. The authorized representative in Taiwan is TRIPLE ROPES ENTERPRISE CO., LTD..
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