Taiwan FDA registration d5e8be5464bc7993f3030b6dd1d07124
"Ailang" contrast agent syringe
TW: “愛琅”造影劑注射筒
Taiwan·Risk Class 2·ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE LTD.·Registered Jan 12, 2001 – Jan 12, 2016CancelledRegistration details
- Analysis ID
- d5e8be5464bc7993f3030b6dd1d07124
- Customs Code
- DHA00600959102
Company information
- Manufacturer
- ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE LTD.
- Manufacturer Country
- Singapore
- Authorized Representative
- EMIND BIOTECH MR CO., LTD.
Product details
- Product Type (Level 1)
- E000 of the 100,000.
- Import Information
- import
Dates and status
- Registration Date
- Jan 12, 2001
- Expiry Date
- Jan 12, 2016
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ailang" contrast agent syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d5e8be5464bc7993f3030b6dd1d07124 and manufactured by ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE LTD.. The authorized representative in Taiwan is EMIND BIOTECH MR CO., LTD..
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