Taiwan FDA registration 0fe13e877e9367d5d226074fcd165a5d

"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 Dec 23, 2013 – Dec 23, 2018Cancelled
Registration details
Analysis ID
0fe13e877e9367d5d226074fcd165a5d
License Form
Ministry of Health Medical Device Import No. 013714
Customs Code
DHA09401371407
Company information
Manufacturer Country
United States
Authorized Representative
Qiatai Enterprise Co., Ltd
Product details
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
Dec 23, 2013
Expiry Date
Dec 23, 2018
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

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 0fe13e877e9367d5d226074fcd165a5d and manufactured by IZI MEDICAL PRODUCTS, LLC. The authorized representative in Taiwan is Qiatai Enterprise Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including IZI MEDICAL PRODUCTS, LLC, 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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