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"MANI" Plup Canal Files (Non-Sterile) - Taiwan Registration 991ddc91374f5734905721a33c13f47e

Access comprehensive regulatory information for "MANI" Plup Canal Files (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 991ddc91374f5734905721a33c13f47e and manufactured by MANI, INC.. The authorized representative in Taiwan is ROLENCE ENTERPRISE 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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991ddc91374f5734905721a33c13f47e
Registration Details
Taiwan FDA Registration: 991ddc91374f5734905721a33c13f47e
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Device Details

"MANI" Plup Canal Files (Non-Sterile)
TW: "้ฆฌๅฐผ" ๆ น็ฎก้Šผ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

991ddc91374f5734905721a33c13f47e

Ministry of Health Medical Device Import No. 016652

DHA09401665200

Company Information

Japan

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".

F Dental devices

F4565 Hand instruments for dental use

Imported from abroad

Dates and Status

Jun 15, 2016

Jun 15, 2021