Taiwan FDA registration 006c5b31ef86fd43e4e317cdae0ff4f0
"Ruida" manual instruments for general surgery (unsterilized)
TW: "瑞達"一般手術用手動式器械(未滅菌)
Registration details
- Analysis ID
- 006c5b31ef86fd43e4e317cdae0ff4f0
- Customs Code
- DHA04400352100
Company information
- Manufacturer
- REDA INSTRUMENTE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Liren Equipment Factory Co., Ltd
Product details
- Intended Use
- It is limited to the scope of first-level identification of medical equipment management measures (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
- Apr 12, 2006
- Expiry Date
- Apr 12, 2011
- Cancellation Date
- Jan 17, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ruida" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 006c5b31ef86fd43e4e317cdae0ff4f0 and manufactured by REDA INSTRUMENTE GMBH. The authorized representative in Taiwan is Liren Equipment Factory Co., 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