Taiwan FDA registration 086558ac5b463d50d8ddaf11d50e5021
"Termao" Ge Lai guide the set
TW: “泰爾茂”葛來引導套
Taiwan·Risk Class 2·TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Oct 23, 2015 – Oct 23, 2025ExpiredRegistration details
- Analysis ID
- 086558ac5b463d50d8ddaf11d50e5021
- Customs Code
- DHA05602776504
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1340 Catheter Introducers
- Import Information
- import
Dates and status
- Registration Date
- Oct 23, 2015
- Expiry Date
- Oct 23, 2025
About this record
Access comprehensive regulatory information for "Termao" Ge Lai guide the set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 086558ac5b463d50d8ddaf11d50e5021 and manufactured by TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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