Taiwan FDA registration c4f1b15e406363a3e9505b47771258c4
“Argon” Pro-Mag Ultra Automatic Biopsy Instrument
TW: “亞康恩”剖美克全自動組織切片器
Taiwan·Risk Class 2·MD·ARGON MEDICAL DEVICES INC.·Registered Jan 05, 2015 – Jan 05, 2025ExpiredRegistration details
- Analysis ID
- c4f1b15e406363a3e9505b47771258c4
- License Form
- Ministry of Health Medical Device Import No. 026897
- Customs Code
- DHA05602689703
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)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1075 Gastroenterology - Urology biopsy instruments
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 05, 2015
- Expiry Date
- Jan 05, 2025
About this record
Access comprehensive regulatory information for “Argon” Pro-Mag Ultra Automatic Biopsy Instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c4f1b15e406363a3e9505b47771258c4 and manufactured by ARGON MEDICAL DEVICES INC.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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