"Termao" Di Di Xun guide set
Taiwan·Risk Class 2·TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Jan 18, 2019 – Jan 18, 2024Expired- Analysis ID
- 211428be3733b8f3593ea2dd03496f9b
- Customs Code
- DHA05603207805
- Manufacturer Country
- Japan
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
- 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
- Registration Date
- Jan 18, 2019
- Expiry Date
- Jan 18, 2024
Top companies providing products similar to ""Termao" Di Di Xun guide set"
Recently registered similar products
Access comprehensive regulatory information for "Termao" Di Di Xun guide set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 211428be3733b8f3593ea2dd03496f9b and manufactured by TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION, and 1 recent registrations in the same category. 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.