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“ENDO-FLEX” Self-Expanding Nitinol Stents - Taiwan Registration dda4201e01b8d06b7f04a4fa6fef8c18

Access comprehensive regulatory information for “ENDO-FLEX” Self-Expanding Nitinol Stents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dda4201e01b8d06b7f04a4fa6fef8c18 and manufactured by ENDO-FLEX GmbH. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).

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dda4201e01b8d06b7f04a4fa6fef8c18
Registration Details
Taiwan FDA Registration: dda4201e01b8d06b7f04a4fa6fef8c18
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Device Details

“ENDO-FLEX” Self-Expanding Nitinol Stents
TW: “福萊克斯”十二指腸-結腸/直腸自擴式支架系統
Risk Class 2
MD

Registration Details

dda4201e01b8d06b7f04a4fa6fef8c18

Ministry of Health Medical Device Import No. 025473

DHA05602547307

Company Information

Product Details

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

I General and plastic surgical devices

I3610 Esophageal supplements

Imported from abroad

Dates and Status

Sep 18, 2013

Sep 18, 2023