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Guide sheath sleeve - Taiwan Registration 76300197495d374cd4f3ba7d63e346c6

Access comprehensive regulatory information for Guide sheath sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 76300197495d374cd4f3ba7d63e346c6 and manufactured by Togo Medikit Co., Ltd. Hyuga Factory;; Togo Medikit Co., Ltd.. The authorized representative in Taiwan is CHINA HOSMED INTERNATIONAL INC..

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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76300197495d374cd4f3ba7d63e346c6
Registration Details
Taiwan FDA Registration: 76300197495d374cd4f3ba7d63e346c6
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Device Details

Guide sheath sleeve
TW: ๅฐŽๅผ•้™„้ž˜ๅฅ—
Risk Class 2

Registration Details

76300197495d374cd4f3ba7d63e346c6

DHA00600973806

Product Details

E000 of the 100,000.

import

Dates and Status

Sep 19, 2001

Sep 19, 2026