Taiwan FDA registration 8a25e36205a98a6e9e7bc69063a930a3
“Argon” Super Core Semi-Automatic Biopsy Instrument
TW: “亞康恩”舒普克半自動組織切片器
Taiwan·Risk Class 2·MD·ARGON MEDICAL DEVICES, INC.·Registered Nov 04, 2014 – Nov 04, 2024ExpiredRegistration details
- Analysis ID
- 8a25e36205a98a6e9e7bc69063a930a3
- License Form
- Ministry of Health Medical Device Import No. 026771
- Customs Code
- DHA05602677107
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
- Nov 04, 2014
- Expiry Date
- Nov 04, 2024
About this record
Access comprehensive regulatory information for “Argon” Super Core Semi-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 8a25e36205a98a6e9e7bc69063a930a3 and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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