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"EMI" Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration 18425ae3be44ac5507d4238a433df3cf

Access comprehensive regulatory information for "EMI" 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 18425ae3be44ac5507d4238a433df3cf and manufactured by EMI FACTORY CO., LTD.. The authorized representative in Taiwan is EVOLUTION WORLDWIDE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including EMI FACTORY CO., LTD., and 1 recent registrations in the same category. 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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18425ae3be44ac5507d4238a433df3cf
Registration Details
Taiwan FDA Registration: 18425ae3be44ac5507d4238a433df3cf
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Device Details

"EMI" Manual surgical instrument for general use (Non-Sterile)
TW: "ๆ˜“ๆฉ่‰พ" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

18425ae3be44ac5507d4238a433df3cf

Ministry of Health Medical Device Import No. 017711

DHA09401771108

Company Information

Japan

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Apr 14, 2017

Apr 14, 2022

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