Taiwan FDA registration 7d055f38f616fbae46129c2fd1cc7c2c
"Ruifeng" powder-free test gloves (non-sterile)
TW: "瑞豐" 無粉檢驗手套 (未滅菌)
Taiwan·Risk Class 1·EN. ARISTA LATINDO·Registered Jan 31, 2024 – Jan 31, 2029ActiveRegistration details
- Analysis ID
- 7d055f38f616fbae46129c2fd1cc7c2c
- Customs Code
- DHA09402338609
Company information
- Manufacturer
- EN. ARISTA LATINDO
- Manufacturer Country
- Indonesia
- Authorized Representative
- RUEY FENG MEDICINE CO., LTD.
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 31, 2024
- Expiry Date
- Jan 31, 2029
About this record
Access comprehensive regulatory information for "Ruifeng" powder-free test gloves (non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7d055f38f616fbae46129c2fd1cc7c2c and manufactured by EN. ARISTA LATINDO. The authorized representative in Taiwan is RUEY FENG MEDICINE CO., LTD..
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