Taiwan FDA registration 0afcfdf802ccc73b512a60a7ac88747f

"Fujifilm" electronic bronchoscope and accessories

TW: “富士”電子式支氣管鏡及附件
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION·Registered Oct 13, 2021 – Oct 13, 2026Active
Registration details
Analysis ID
0afcfdf802ccc73b512a60a7ac88747f
Customs Code
DHA05603497302
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)
G ENT Science
Product Type (Level 2)
G.4680 Bronchial tubescopes (soft or rigid) and accessories thereof
Import Information
import
Dates and status
Registration Date
Oct 13, 2021
Expiry Date
Oct 13, 2026
About this record

Access comprehensive regulatory information for "Fujifilm" electronic bronchoscope 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 0afcfdf802ccc73b512a60a7ac88747f 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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