Taiwan FDA registration 3212fe2c6496514ae915f070187015c9
Shisei's Patient Examination Gloves (Powder-Free) (Non-Sterilized)
TW: "資生" 病患檢查用手套(無粉)(未滅菌)
Taiwan·Risk Class 1·MAXTER GLOVE MANUFACTURING SDN. BHD.·Registered Jan 23, 2024 – Jan 23, 2029ActiveRegistration details
- Analysis ID
- 3212fe2c6496514ae915f070187015c9
- Customs Code
- DHA09402337504
Company information
- Manufacturer
- MAXTER GLOVE MANUFACTURING SDN. BHD.
- Manufacturer Country
- Malaysia
- Authorized Representative
- SHI SEI INTERNATIONAL LIMITED
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Classification and Grading of Medical Equipment "Gloves for Patient Examination (J.6250)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6250 病患檢查用手套
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jan 23, 2024
- Expiry Date
- Jan 23, 2029
About this record
Access comprehensive regulatory information for Shisei's Patient Examination Gloves (Powder-Free) (Non-Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3212fe2c6496514ae915f070187015c9 and manufactured by MAXTER GLOVE MANUFACTURING SDN. BHD.. The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.
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