Taiwan FDA registration 7745b649d26526f01b650bb24bff183e
“Argon” Retrievable Vena Cave Filter
TW: “雅客”可回收血栓過濾網
Taiwan·Risk Class 2·MD·ARGON MEDICAL DEVICES, INC.·Registered Mar 12, 2018 – Mar 12, 2028ActiveRegistration details
- Analysis ID
- 7745b649d26526f01b650bb24bff183e
- License Form
- Ministry of Health Medical Device Import No. 030760
- Customs Code
- DHA05603076004
Company information
- Manufacturer
- ARGON MEDICAL DEVICES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- JENS MEDICAL CONSULTING 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)
- E3375 Cardiovascular endovascular filter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 12, 2018
- Expiry Date
- Mar 12, 2028
About this record
Access comprehensive regulatory information for “Argon” Retrievable Vena Cave Filter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7745b649d26526f01b650bb24bff183e and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is JENS MEDICAL CONSULTING LTD..
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