Taiwan FDA registration 0f5c65aa49b3b18c52e2ee8bf86d47e0
"Guanda" examination gloves (powder-free) (sterilized/non-sterile)
TW: “觀達”檢診手套 (無粉)(滅菌/未滅菌)
Registration details
- Analysis ID
- 0f5c65aa49b3b18c52e2ee8bf86d47e0
- Customs Code
- DHA09401351705
Company information
- Manufacturer Country
- Thailand
- Authorized Representative
- GRAND KTTA 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
- Oct 21, 2013
- Expiry Date
- Oct 21, 2028
About this record
Access comprehensive regulatory information for "Guanda" examination gloves (powder-free) (sterilized/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 0f5c65aa49b3b18c52e2ee8bf86d47e0 and manufactured by SRI TRANG GLOVES (THAILAND) PUBLIC COMPANY LIMITED. The authorized representative in Taiwan is GRAND KTTA 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