Taiwan FDA registration bcfcd8657accbe44a8300192df6ad12e

"IZI" Obstetric-Gynecologic General Manual Instrument (Non-sterile)

TW: "愛立艾"婦產科用一般手動器械(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·IZI MEDICAL PRODUCTS, LLC·Registered Apr 12, 2019 – Apr 12, 2024Expired
Registration details
Analysis ID
bcfcd8657accbe44a8300192df6ad12e
License Form
Ministry of Health Medical Device Import No. 020310
Customs Code
DHA09402031000
Company information
Manufacturer Country
United States
Authorized Representative
Cooperative L.F. Enterprise Co.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "General Manual Instruments for Obstetrics and Gynecology (L.4520)".
Product Type (Level 1)
l Devices for obstetrics and gynecology
Product Type (Level 2)
L4520 General manual instruments for obstetrics and gynecology
Import Information
Imported from abroad
Dates and status
Registration Date
Apr 12, 2019
Expiry Date
Apr 12, 2024
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Access comprehensive regulatory information for "IZI" Obstetric-Gynecologic General Manual Instrument (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 bcfcd8657accbe44a8300192df6ad12e and manufactured by IZI MEDICAL PRODUCTS, LLC. The authorized representative in Taiwan is Cooperative L.F. Enterprise Co..

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