"IZI" Rectal Dilator (Non-sterile)
- Analysis ID
- 75ef7ccab9ee9a4599028e017e818929
- License Form
- Ministry of Health Medical Device Import No. 020309
- Customs Code
- DHA09402030902
- Manufacturer
- IZI MEDICAL PRODUCTS, LLC
- Manufacturer Country
- United States
- Authorized Representative
- Cooperative L.F. Enterprise Co.
- 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
- Registration Date
- Apr 12, 2019
- Expiry Date
- Apr 12, 2024
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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.