Taiwan FDA registration d0a02b8df5fcd4d4d31d79fa25c1d3db
"Morse Reilai" manual instruments for general surgery (sterilization)
TW: "摩斯 瑞來" 一般手術用手動式器械 (滅菌)
Taiwan·Risk Class 1·MORPHEUS AG·Registered Mar 03, 2021 – Mar 03, 2026ExpiredRegistration details
- Analysis ID
- d0a02b8df5fcd4d4d31d79fa25c1d3db
- Customs Code
- DHA09402235101
Company information
- Manufacturer
- MORPHEUS AG
- Manufacturer Country
- Germany
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
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
- Mar 03, 2021
- Expiry Date
- Mar 03, 2026
About this record
Access comprehensive regulatory information for "Morse Reilai" manual instruments for general surgery (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d0a02b8df5fcd4d4d31d79fa25c1d3db and manufactured by MORPHEUS AG. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
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