Taiwan FDA registration f959cfcd1a2f8bca6020d78a77dddcbd

"EMI" Manual Surgical Instrument for General Use (Non-sterile)

TW: "尹恩艾" 一般手術用手動式器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·EMI FACTORY CO., LTD.·Registered Jul 19, 2018 – Jul 19, 2023Expired
Registration details
Analysis ID
f959cfcd1a2f8bca6020d78a77dddcbd
License Form
Ministry of Health Medical Device Import No. 019332
Customs Code
DHA09401933200
Company information
Manufacturer Country
Japan
Authorized Representative
GEMMGTAI CO.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1)
I General and plastic surgical devices
Product Type (Level 2)
I4800 General Surgery Manual Instrument
Import Information
Imported from abroad
Dates and status
Registration Date
Jul 19, 2018
Expiry Date
Jul 19, 2023
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About this record

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 f959cfcd1a2f8bca6020d78a77dddcbd and manufactured by EMI FACTORY CO., LTD.. The authorized representative in Taiwan is GEMMGTAI CO..

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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