Taiwan FDA registration b4f761baed945a84940bcbbb9e8dafbb
“Argon” Jawz Endomyocardial Biopsy Forceps
TW: “亞康恩”久茲心臟內膜活體組織夾
Taiwan·Risk Class 2·MD·ARGON MEDICAL DEVICES, INC.·Registered Dec 19, 2019 – Dec 19, 2024ExpiredRegistration details
- Analysis ID
- b4f761baed945a84940bcbbb9e8dafbb
- License Form
- Ministry of Health Medical Device Import No. 033070
- Customs Code
- DHA05603307007
Company information
- Manufacturer
- ARGON MEDICAL DEVICES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- CHINA SPRING TRADING CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E4075 Endocardial sectioning device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 19, 2019
- Expiry Date
- Dec 19, 2024
About this record
Access comprehensive regulatory information for “Argon” Jawz Endomyocardial Biopsy Forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b4f761baed945a84940bcbbb9e8dafbb and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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