Taiwan FDA registration 7954d8c2cd69848964af7616ff97c86b
"Leach" surgical instruments, motors with accessories or accessories (unsterilized)
TW: “利奇”手術用器具馬達與配件或附件 (未滅菌)
Taiwan·Risk Class 1·REGEN LAB SA·Registered Jul 05, 2012 – Jul 05, 2017CancelledRegistration details
- Analysis ID
- 7954d8c2cd69848964af7616ff97c86b
- Customs Code
- DHA04401191402
Company information
- Manufacturer
- REGEN LAB SA
- Manufacturer Country
- Switzerland
- Authorized Representative
- NEOASIA LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Surgical Instruments, Motors and Accessories or Accessories (I.4820)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4820 Surgical Appliances and Accessories or Accessories
- Import Information
- import
Dates and status
- Registration Date
- Jul 05, 2012
- Expiry Date
- Jul 05, 2017
- Cancellation Date
- Jul 13, 2015
Cancellation information
- Status
- Logged out
- Reason
- 效能逾越等級範圍
About this record
Access comprehensive regulatory information for "Leach" surgical instruments, motors with accessories or accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7954d8c2cd69848964af7616ff97c86b and manufactured by REGEN LAB SA. The authorized representative in Taiwan is NEOASIA LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices