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GORE EXCLUDER Iliac Branch Endoprosthesis - Taiwan Registration 89402d5841eb28f98b558ae220b6eb70

Access comprehensive regulatory information for GORE EXCLUDER Iliac Branch Endoprosthesis in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 89402d5841eb28f98b558ae220b6eb70 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.).

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89402d5841eb28f98b558ae220b6eb70
Registration Details
Taiwan FDA Registration: 89402d5841eb28f98b558ae220b6eb70
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Device Details

GORE EXCLUDER Iliac Branch Endoprosthesis
TW: โ€œๆˆˆ็ˆพโ€ๆ˜“ๆ™‚ๅ›บๅพ—้ซ‚ๅ‹•่„ˆๅˆ†ๆ”ฏ่ก€็ฎกๆ”ฏๆžถ
Risk Class 3
MD

Registration Details

89402d5841eb28f98b558ae220b6eb70

Ministry of Health Medical Device Import No. 032063

DHA05603206305

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E0006 Endovascular Transplantation System

Imported from abroad; The use of this equipment shall comply with the "Administrative Measures for the Implementation or Use of Specific Medical Technical Examination and Inspection Medical Equipment"

Dates and Status

Jan 04, 2019

Jan 04, 2029