Taiwan FDA registration eea5c2e0284f1fd45dc46ceee28c5d20
"Angelmed" Urosu tumor ureteral stent group
TW: “安吉美爾德”優柔舒腫瘤輸尿管支架組
Taiwan·Risk Class 2·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Registered Jul 01, 2012 – Jul 01, 2027ActiveRegistration details
- Analysis ID
- eea5c2e0284f1fd45dc46ceee28c5d20
- Customs Code
- DHA00602369509
Company information
- Manufacturer
- ANGIOMED GMBH & CO. MEDIZINTECHNIK KG
- Manufacturer Country
- Germany
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.4620 Urinary Catheter Stent
- Import Information
- import
Dates and status
- Registration Date
- Jul 01, 2012
- Expiry Date
- Jul 01, 2027
About this record
Access comprehensive regulatory information for "Angelmed" Urosu tumor ureteral stent group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eea5c2e0284f1fd45dc46ceee28c5d20 and manufactured by ANGIOMED GMBH & CO. MEDIZINTECHNIK KG. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE 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