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"FUJIFILM" Manual Surgical Instrument for General Use (Non-Sterile) - Taiwan Registration 00d7e10f918f12bcb3351c2c5c9226f0

Access comprehensive regulatory information for "FUJIFILM" Manual Surgical Instrument for General Use (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 00d7e10f918f12bcb3351c2c5c9226f0 and manufactured by FUJIFILM CORPORATION. The authorized representative in Taiwan is WELMORE CO., LTD..

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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00d7e10f918f12bcb3351c2c5c9226f0
Registration Details
Taiwan FDA Registration: 00d7e10f918f12bcb3351c2c5c9226f0
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Device Details

"FUJIFILM" Manual Surgical Instrument for General Use (Non-Sterile)
TW: "ๅฏŒๅฃซ" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

00d7e10f918f12bcb3351c2c5c9226f0

Ministry of Health Medical Device Import No. 015630

DHA09401563001

Company Information

Japan

Product Details

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Sep 01, 2015

Sep 01, 2020

Jun 22, 2022

Cancellation Information

Logged out

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