Taiwan FDA registration 75ef7ccab9ee9a4599028e017e818929

"IZI" Rectal Dilator (Non-sterile)

TW: "愛立艾"直腸擴張器(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·IZI MEDICAL PRODUCTS, LLC·Registered Apr 12, 2019 – Apr 12, 2024Expired
Registration details
Analysis ID
75ef7ccab9ee9a4599028e017e818929
License Form
Ministry of Health Medical Device Import No. 020309
Customs Code
DHA09402030902
Company information
Manufacturer Country
United States
Authorized Representative
Cooperative L.F. Enterprise Co.
Product details
Intended Use
Limited to the first level identification range of "rectal dilator (H.5450)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
H Gastroenterology-urology devices
Product Type (Level 2)
H5450 Rectal dilators
Import Information
Imported from abroad
Dates and status
Registration Date
Apr 12, 2019
Expiry Date
Apr 12, 2024
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About this record

Access comprehensive regulatory information for "IZI" Rectal Dilator (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 75ef7ccab9ee9a4599028e017e818929 and manufactured by IZI MEDICAL PRODUCTS, LLC. The authorized representative in Taiwan is Cooperative L.F. Enterprise Co..

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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