Taiwan FDA registration f6440b9f9b37091061863fd1149747b6
"Baxter" adjustable endoscopic application catheter
TW: “百特”可調整式內視鏡應用導管
Taiwan·Risk Class 2·Made (部分製程) in MEXICO;; MICROMEDICS, INC.·Registered Feb 16, 2020 – Feb 16, 2030ActiveRegistration details
- Analysis ID
- f6440b9f9b37091061863fd1149747b6
- Customs Code
- DHA05603320007
Company information
- Manufacturer
- Made (部分製程) in MEXICO;; MICROMEDICS, INC.
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- BAXTER HEALTHCARE LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Feb 16, 2020
- Expiry Date
- Feb 16, 2030
About this record
Access comprehensive regulatory information for "Baxter" adjustable endoscopic application catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f6440b9f9b37091061863fd1149747b6 and manufactured by Made (部分製程) in MEXICO;; MICROMEDICS, INC.. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
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