Taiwan FDA registration 0b653cd5a182a6404b38234857e76ffd

"Gore" thoracic aortic aneurysm stent

TW: “戈爾”胸主動脈瘤支架
Taiwan flagTaiwan·Risk Class 3·W.L. GORE & ASSOCIATES INC.·Registered Jun 05, 2014 – Jun 05, 2029Active
Registration details
Analysis ID
0b653cd5a182a6404b38234857e76ffd
Customs Code
DHA05602622506
Company information
Manufacturer Country
United States
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.0001 Cardiovascular stents
Import Information
Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
Dates and status
Registration Date
Jun 05, 2014
Expiry Date
Jun 05, 2029
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About this record

Access comprehensive regulatory information for "Gore" thoracic aortic aneurysm stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0b653cd5a182a6404b38234857e76ffd and manufactured by W.L. GORE & ASSOCIATES INC.. The authorized representative in Taiwan is W.L. GORE & ASSOCIATES (HONG KONG) LTD. TAIWAN BRANCH (H.K.).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including W.L. GORE & ASSOCIATES INC., 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.

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