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"Taiwan Advanced" Rectal Dilator (Unsterilized) - Taiwan Registration e1f2dc5d7803877290c52b7e99b2fe52

Access comprehensive regulatory information for "Taiwan Advanced" Rectal Dilator (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e1f2dc5d7803877290c52b7e99b2fe52 and manufactured by TAIWAN SURGICAL CORPORATION. The authorized representative in Taiwan is TAIWAN SURGICAL CORPORATION.

This page provides complete technical specifications, regulatory compliance details. 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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e1f2dc5d7803877290c52b7e99b2fe52
Registration Details
Taiwan FDA Registration: e1f2dc5d7803877290c52b7e99b2fe52
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Device Details

"Taiwan Advanced" Rectal Dilator (Unsterilized)
TW: "ๅฐ็ฃๅ…ˆ้€ฒ" ็›ด่…ธๆ“ดๅผตๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e1f2dc5d7803877290c52b7e99b2fe52

Company Information

Taiwan, Province of China

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 and urology

H.5450 Rectal dilator

Domestic

Dates and Status

Mar 07, 2014

Mar 07, 2019

Aug 05, 2022

Cancellation Information

Logged out

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