Taiwan FDA registration b21c5cc485322afdcd6614808801ab97
“Tru-Core” I Biopsy Needles
TW: “楚克”切片針
Taiwan·Risk Class 2·MD·ARGON MEDICAL DEVICES, INC.·Registered Oct 24, 2013 – Oct 24, 2023ExpiredRegistration details
- Analysis ID
- b21c5cc485322afdcd6614808801ab97
- License Form
- Ministry of Health Medical Device Import No. 025507
- Customs Code
- DHA05602550701
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
- Oct 24, 2013
- Expiry Date
- Oct 24, 2023
About this record
Access comprehensive regulatory information for “Tru-Core” I Biopsy Needles in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b21c5cc485322afdcd6614808801ab97 and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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