Taiwan FDA registration 54e0678da4f661c4aaa6f0a178f8435f
"Meritt" Flow arteriovenous tube with a guide sheath
TW: “美瑞特”福祿動靜脈廔管用導引鞘
Taiwan·Risk Class 2·MERIT MEDICAL SYSTEMS, INC.·Registered May 19, 2010 – May 19, 2030ActiveRegistration details
- Analysis ID
- 54e0678da4f661c4aaa6f0a178f8435f
- Customs Code
- DHA00602103305
Company information
- Manufacturer
- MERIT MEDICAL SYSTEMS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Merit Medical Asia Company Limited Taiwan Branch (Hong Kong)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1310 經皮導管用血管擴張器
- Import Information
- import
Dates and status
- Registration Date
- May 19, 2010
- Expiry Date
- May 19, 2030
About this record
Access comprehensive regulatory information for "Meritt" Flow arteriovenous tube with a guide sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 54e0678da4f661c4aaa6f0a178f8435f and manufactured by MERIT MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is Merit Medical Asia Company Limited Taiwan Branch (Hong Kong).
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