Taiwan FDA registration a10a76cde4be8ad310ef8b4e2aac6f7a
"Fuji" Terpo Infusion Gangpu
TW: "富士" 特浦輸液幫浦
Taiwan·Risk Class 2·FUJI ELECTRIC F-TECH CO., LTD.;; TOP CORPORATION·Registered Sep 18, 2003 – Sep 18, 2018CancelledRegistration details
- Analysis ID
- a10a76cde4be8ad310ef8b4e2aac6f7a
- Customs Code
- DHA00601040008
Company information
- Manufacturer
- FUJI ELECTRIC F-TECH CO., LTD.;; TOP CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- Taiwan TPU Co., Ltd
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Import Information
- import
Dates and status
- Registration Date
- Sep 18, 2003
- Expiry Date
- Sep 18, 2018
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fuji" Terpo Infusion Gangpu in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a10a76cde4be8ad310ef8b4e2aac6f7a and manufactured by FUJI ELECTRIC F-TECH CO., LTD.;; TOP CORPORATION. The authorized representative in Taiwan is Taiwan TPU Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices