Taiwan FDA registration f95b59e86ce09cb0f15d8c3b59a095f4
"Mikewei" manual instruments for general surgery (unsterilized)
TW: “邁柯唯”一般手術用手動式器械 (未滅菌)
Registration details
- Analysis ID
- f95b59e86ce09cb0f15d8c3b59a095f4
- Customs Code
- DHA04401032106
Company information
- Manufacturer
- MAQUET GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- 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
- May 06, 2011
- Expiry Date
- May 06, 2026
About this record
Access comprehensive regulatory information for "Mikewei" 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 f95b59e86ce09cb0f15d8c3b59a095f4 and manufactured by MAQUET GMBH. The authorized representative in Taiwan is GETINGE GROUP TAIWAN 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