Taiwan FDA registration 5cd74eaeb6641076cdbefbbc775fc730
"Meiji Card" surgical brush (sterilization)
TW: “美諦卡” 外科用刷手刷子 (滅菌)
Registration details
- Analysis ID
- 5cd74eaeb6641076cdbefbbc775fc730
- Customs Code
- DHA09401998006
Company information
- Manufacturer
- MEDICA EUROPE B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- RECHI 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 28, 2018
- Expiry Date
- Dec 28, 2023
About this record
Access comprehensive regulatory information for "Meiji Card" surgical brush (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5cd74eaeb6641076cdbefbbc775fc730 and manufactured by MEDICA EUROPE B.V.. The authorized representative in Taiwan is RECHI 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.
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