"Shengyouda" longitudinal split external guide tube
- Analysis ID
- 9ef171d8a18619f5782e43e382a9a9c4
- Customs Code
- DHA00601834300
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Shengyuda Medical Supplies 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
- Sep 29, 2007
- Expiry Date
- Sep 29, 2017
- Cancellation Date
- Nov 04, 2019
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Shengyouda" longitudinal split external guide tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ef171d8a18619f5782e43e382a9a9c4 and manufactured by ST. JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION. The authorized representative in Taiwan is Taiwan Shengyuda Medical Supplies Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ST. JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION;; ST. JUDE MEDICAL, 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.