Taiwan FDA registration 24662906435a0a1850df110a9e467cfa

"Endovision" Manual surgical instrument for general use (Non-sterile)

TW: "安朵微視" 一般手術用手動式器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·ENDOVISION CO., LTD·Registered Jun 08, 2018 – Jun 08, 2023Expired
Registration details
Analysis ID
24662906435a0a1850df110a9e467cfa
License Form
Ministry of Health Medical Device Import No. 019159
Customs Code
DHA09401915909
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
ORTHOLAND CORPORATION
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
Jun 08, 2018
Expiry Date
Jun 08, 2023
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About this record

Access comprehensive regulatory information for "Endovision" 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 24662906435a0a1850df110a9e467cfa and manufactured by ENDOVISION CO., LTD. The authorized representative in Taiwan is ORTHOLAND CORPORATION.

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