Taiwan FDA registration 4773ab275cb877972bacc824b2aa0cef
Tepu infusion pump
TW: 特浦輸液幫浦
Taiwan·Risk Class 2·FUJI ELECTRIC F-TECH CO., LTD.;; TOP CORPORATION·Registered Mar 27, 2001 – Mar 27, 2021CancelledRegistration details
- Analysis ID
- 4773ab275cb877972bacc824b2aa0cef
- Customs Code
- DHA00600963601
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)
- J000 General Hospital & Personal Use Devices
- Import Information
- import
Dates and status
- Registration Date
- Mar 27, 2001
- Expiry Date
- Mar 27, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Tepu infusion pump in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4773ab275cb877972bacc824b2aa0cef 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