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"IZI" Rectal Dilator (Non-Sterile) - Taiwan Registration c58d8e0fa00bd7c23b44e7ddcf4a1674

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 c58d8e0fa00bd7c23b44e7ddcf4a1674 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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c58d8e0fa00bd7c23b44e7ddcf4a1674
Registration Details
Taiwan FDA Registration: c58d8e0fa00bd7c23b44e7ddcf4a1674
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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
Cancelled

Registration Details

c58d8e0fa00bd7c23b44e7ddcf4a1674

Ministry of Health Medical Device Import No. 013713

DHA09401371305

Company Information

United States

Product Details

H Gastroenterology-urology devices

H5450 Rectal dilators

Imported from abroad

Dates and Status

Dec 23, 2013

Dec 23, 2018

Jul 15, 2022

Cancellation Information

Logged out

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