Taiwan FDA registration 3b699e4b536f6ab3f08e930ce33a23bf
“Argon” TLAB Transjugular Liver Biopsy System
TW: “亞康恩”提雷伯 經頸靜脈肝切片系統
Taiwan·Risk Class 2·MD·ARGON MEDICAL DEVICES, INC.·Registered Jun 21, 2019 – Jun 21, 2024ExpiredRegistration details
- Analysis ID
- 3b699e4b536f6ab3f08e930ce33a23bf
- License Form
- Ministry of Health Medical Device Import No. 032649
- Customs Code
- DHA05603264909
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)
- E1340 Catheter Guide
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 21, 2019
- Expiry Date
- Jun 21, 2024
About this record
Access comprehensive regulatory information for “Argon” TLAB Transjugular Liver Biopsy System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3b699e4b536f6ab3f08e930ce33a23bf and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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