Taiwan FDA registration 878f3de07a1548b0444465deaf583de3
“RegenLab”Manual surgical instrument for general use (Non-Sterile)
TW: “利奇”一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·REGEN LAB SA·Registered Dec 19, 2013 – Dec 19, 2018CancelledRegistration details
- Analysis ID
- 878f3de07a1548b0444465deaf583de3
- License Form
- Ministry of Health Medical Device Import No. 013699
- Customs Code
- DHA09401369901
Company information
- Manufacturer
- REGEN LAB SA
- Manufacturer Country
- Switzerland
- Authorized Representative
- NEOTEC COSMECEUTICAL LIMITED
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 19, 2013
- Expiry Date
- Dec 19, 2018
- Cancellation Date
- Jul 01, 2015
Cancellation information
- Status
- Logged out
- Reason
- 經查市售品非屬原核准醫療器材鑑別範圍
About this record
Access comprehensive regulatory information for “RegenLab”Manual surgical instrument for general use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 878f3de07a1548b0444465deaf583de3 and manufactured by REGEN LAB SA. The authorized representative in Taiwan is NEOTEC COSMECEUTICAL LIMITED.
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