Taiwan FDA registration f3f9011cee69566e6eecd3130ef16971
"Riqi" manual instrument for general surgery (not sterilized)
TW: “利奇”一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·REGENLAB SARL·Registered Sep 10, 2008 – Sep 10, 2013CancelledRegistration details
- Analysis ID
- f3f9011cee69566e6eecd3130ef16971
- Customs Code
- DHA04400705603
Company information
- Manufacturer
- REGENLAB SARL
- Manufacturer Country
- Switzerland
- Authorized Representative
- NEOTEC COSMECEUTICAL LIMITED
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Sep 10, 2008
- Expiry Date
- Sep 10, 2013
- Cancellation Date
- Aug 04, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Riqi" manual instrument for general surgery (not sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f3f9011cee69566e6eecd3130ef16971 and manufactured by REGENLAB SARL. The authorized representative in Taiwan is NEOTEC COSMECEUTICAL LIMITED.
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