Taiwan FDA registration 12e52e96dccd3ab1056dc38a293e0204

"Fujifilm" rinses the electric knife with high frequency in a single time

TW: “富士”單次用高頻沖洗電刀
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION·Registered Jul 15, 2022 – Jul 15, 2027Active
Registration details
Analysis ID
12e52e96dccd3ab1056dc38a293e0204
Customs Code
DHA05603570702
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.4300 Electrosurgical device for endoscopy and accessories thereof
Import Information
import
Dates and status
Registration Date
Jul 15, 2022
Expiry Date
Jul 15, 2027
About this record

Access comprehensive regulatory information for "Fujifilm" rinses the electric knife with high frequency in a single time in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 12e52e96dccd3ab1056dc38a293e0204 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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