Pure Global

"Fujita" Manual Surgical Instrument for General Use (Non-Sterile) - Taiwan Registration 9e807098e7b40b12227a0c5845e8ba83

Access comprehensive regulatory information for "Fujita" 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 9e807098e7b40b12227a0c5845e8ba83 and manufactured by FUJITA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is MATECH HEALTHCARE CORPORATION.

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
9e807098e7b40b12227a0c5845e8ba83
Registration Details
Taiwan FDA Registration: 9e807098e7b40b12227a0c5845e8ba83
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

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

Registration Details

9e807098e7b40b12227a0c5845e8ba83

Ministry of Health Medical Device Import No. 014351

DHA09401435102

Company Information

Product Details

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Jul 22, 2014

Jul 22, 2019

Jul 15, 2022

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€