Taiwan FDA registration 6acec88b61570e3c428f1fb35a266c70
“Argon” Tru-Core II Automatic Biopsy Instrument
TW: “亞康恩”楚克自動組織切片器
Taiwan·Risk Class 2·MD·ARGON MEDICAL DEVICES INC.·Registered Dec 27, 2014 – Dec 27, 2024ExpiredRegistration details
- Analysis ID
- 6acec88b61570e3c428f1fb35a266c70
- License Form
- Ministry of Health Medical Device Import No. 026885
- Customs Code
- DHA05602688509
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
- Dec 27, 2014
- Expiry Date
- Dec 27, 2024
About this record
Access comprehensive regulatory information for “Argon” Tru-Core II 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 6acec88b61570e3c428f1fb35a266c70 and manufactured by ARGON MEDICAL DEVICES INC.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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