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"IZI" Rectal Dilator (Non-sterile) - Taiwan Registration 75ef7ccab9ee9a4599028e017e818929

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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75ef7ccab9ee9a4599028e017e818929
Registration Details
Taiwan FDA Registration: 75ef7ccab9ee9a4599028e017e818929
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Device Details

"IZI" Rectal Dilator (Non-sterile)
TW: "ๆ„›็ซ‹่‰พ"็›ด่…ธๆ“ดๅผตๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

75ef7ccab9ee9a4599028e017e818929

Ministry of Health Medical Device Import No. 020309

DHA09402030902

Company Information

United States

Product Details

Limited to the first level identification range of "rectal dilator (H.5450)" of the Measures for the Administration of Medical Devices.

H Gastroenterology-urology devices

H5450 Rectal dilators

Imported from abroad

Dates and Status

Apr 12, 2019

Apr 12, 2024

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