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"Flex" bracket placement kit - Taiwan Registration b76d18ab3be3d8950ea4d976ef570f21

Access comprehensive regulatory information for "Flex" bracket placement kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b76d18ab3be3d8950ea4d976ef570f21 and manufactured by ENDO-FLEX GMBH. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).

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.

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b76d18ab3be3d8950ea4d976ef570f21
Registration Details
Taiwan FDA Registration: b76d18ab3be3d8950ea4d976ef570f21
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Device Details

"Flex" bracket placement kit
TW: โ€œ็ฆ่Šๅ…‹ๆ–ฏโ€ๆ”ฏๆžถๆ”พ็ฝฎๅฅ—็ต„
Risk Class 2

Registration Details

b76d18ab3be3d8950ea4d976ef570f21

DHA00601984401

Company Information

Product Details

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

H Gastroenterology and urology

H.5010 ่†ฝ็ฎก็”จๅฐŽ็ฎกๅŠๅ…ถ้™„ไปถ

import

Dates and Status

May 12, 2009

May 12, 2024