Taiwan FDA registration 00d7e10f918f12bcb3351c2c5c9226f0
"FUJIFILM" Manual Surgical Instrument for General Use (Non-Sterile)
TW: "富士" 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·FUJIFILM CORPORATION·Registered Sep 01, 2015 – Sep 01, 2020CancelledRegistration details
- Analysis ID
- 00d7e10f918f12bcb3351c2c5c9226f0
- License Form
- Ministry of Health Medical Device Import No. 015630
- Customs Code
- DHA09401563001
Company information
- Manufacturer
- FUJIFILM CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- WELMORE CO., LTD.
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 01, 2015
- Expiry Date
- Sep 01, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "FUJIFILM" Manual Surgical Instrument for General Use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 00d7e10f918f12bcb3351c2c5c9226f0 and manufactured by FUJIFILM CORPORATION. The authorized representative in Taiwan is WELMORE CO., LTD..
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