Taiwan FDA registration 4b68b2f51d9fb1f87f5fb284264b4c30

"Fujifilm" ultrasound endoscope airbag (unsterilized)

TW: “富士”超音波內視鏡用氣囊(未滅菌)
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION·Registered May 23, 2018 – May 23, 2028Active
Registration details
Analysis ID
4b68b2f51d9fb1f87f5fb284264b4c30
Customs Code
DHA05603109309
Company information
Manufacturer Country
Japan
Authorized Representative
FUJIFILM HEALTHCARE TAIWAN CO., 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
May 23, 2018
Expiry Date
May 23, 2028
About this record

Access comprehensive regulatory information for "Fujifilm" ultrasound endoscope airbag (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b68b2f51d9fb1f87f5fb284264b4c30 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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