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"Flex" photo tube - Taiwan Registration 8efc6690805c1f0fad5879ed3cf262f3

Access comprehensive regulatory information for "Flex" photo tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8efc6690805c1f0fad5879ed3cf262f3 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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8efc6690805c1f0fad5879ed3cf262f3
Registration Details
Taiwan FDA Registration: 8efc6690805c1f0fad5879ed3cf262f3
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Device Details

"Flex" photo tube
TW: โ€œ็ฆ่Šๅ…‹ๆ–ฏโ€้€ ๅฝฑ็ฎก
Risk Class 2

Registration Details

8efc6690805c1f0fad5879ed3cf262f3

DHA00601795306

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

Mar 22, 2007

Mar 22, 2022