Taiwan FDA registration 6d4d9390840cf614f51186db740e0769
“Hemcon” Patch PRO
TW: “漢康”止血貼布
Taiwan·Risk Class 3·MD·Tricol Biomedical, INC.·Registered Jun 09, 2017 – Jun 09, 2022ExpiredRegistration details
- Analysis ID
- 6d4d9390840cf614f51186db740e0769
- License Form
- Ministry of Health Medical Device Import No. 029744
- Customs Code
- DHA05602974406
Company information
- Manufacturer
- Tricol Biomedical, INC.
- Manufacturer Country
- United States
- Authorized Representative
- YUANTECH MEDICAL INC.
Product details
- Intended Use
- This product is applied externally to the human body, which can temporarily control hemostasis in emergency situations, and can also be used for dialysis, percutaneous needle puncture or percutaneous catheter wound to stop bleeding.
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4490 Absorbable hemostatic agents and dressings
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 09, 2017
- Expiry Date
- Jun 09, 2022
About this record
Access comprehensive regulatory information for “Hemcon” Patch PRO in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 6d4d9390840cf614f51186db740e0769 and manufactured by Tricol Biomedical, INC.. The authorized representative in Taiwan is YUANTECH MEDICAL INC..
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