"Termao" Di Di Xun guide set
Taiwan·Risk Class 2·TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Jul 19, 2010 – Jul 19, 2015Cancelled- Analysis ID
- a43410a7851609c9d6927061c8584b17
- Customs Code
- DHA00602125905
- Manufacturer Country
- Japan
- Authorized Representative
- Taipei Branch of Nissho Termo 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.1250 Percutaneous catheters
- Import Information
- import
- Registration Date
- Jul 19, 2010
- Expiry Date
- Jul 19, 2015
- Cancellation Date
- Aug 19, 2016
- Status
- Logged out
- Reason
- 公司歇業
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 a43410a7851609c9d6927061c8584b17 and manufactured by TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is Taipei Branch of Nissho Termo 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.