Taiwan FDA registration c6d5001f72fadb02fe0ff6d10573ae3a
"GI" SPOT ENDOSCOPIC MARKER
TW: "吉愛" 史斑特內視鏡記號液
Taiwan·Risk Class 2·MD·GI SUPPLY·Registered Feb 22, 2005 – Feb 22, 2025ExpiredRegistration details
- Analysis ID
- c6d5001f72fadb02fe0ff6d10573ae3a
- License Form
- Department of Health Medical Device Import No. 011058
- Customs Code
- DHA00601105802
Company information
- Manufacturer
- GI SUPPLY
- Manufacturer Country
- United States
- Authorized Representative
- IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 22, 2005
- Expiry Date
- Feb 22, 2025
About this record
Access comprehensive regulatory information for "GI" SPOT ENDOSCOPIC MARKER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c6d5001f72fadb02fe0ff6d10573ae3a and manufactured by GI SUPPLY. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).
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