Taiwan FDA registration 31a185605ae89d0d521d67da4a9a8056

"OMNIA" Manual surgical instrument for general use (Non-Sterile)

TW: "歐尼雅" 一般手術用手動式器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·OMNIA·Registered Feb 24, 2016 – Feb 24, 2021Expired
Registration details
Analysis ID
31a185605ae89d0d521d67da4a9a8056
License Form
Ministry of Health Medical Device Import No. 016185
Customs Code
DHA09401618508
Company information
Manufacturer
OMNIA
Manufacturer Country
Italy
Authorized Representative
YUYING BIOTECHNOLOGY CO., LTD.
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
Feb 24, 2016
Expiry Date
Feb 24, 2021
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About this record

Access comprehensive regulatory information for "OMNIA" 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 31a185605ae89d0d521d67da4a9a8056 and manufactured by OMNIA. The authorized representative in Taiwan is YUYING BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including OMNIA, 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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