Taiwan FDA registration 6a446516f34cd4d6aa96810906ba9f74

"Fujifilm" ultrasound endoscope and accessories

TW: “富士”超音波內視鏡及附件
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION·Registered Oct 07, 2022 – Oct 07, 2027Active
Registration details
Analysis ID
6a446516f34cd4d6aa96810906ba9f74
Customs Code
DHA05603592509
Company information
Manufacturer Country
Japan
Authorized Representative
FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
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
Oct 07, 2022
Expiry Date
Oct 07, 2027
About this record

Access comprehensive regulatory information for "Fujifilm" ultrasound endoscope and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6a446516f34cd4d6aa96810906ba9f74 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

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