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"ASTF" cold compress (unsterilized) - Taiwan Registration 9614f926daf63c383832457d20799fb4

Access comprehensive regulatory information for "ASTF" cold compress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9614f926daf63c383832457d20799fb4 and manufactured by VENICE LABORATORIES CO., LTD.. The authorized representative in Taiwan is HON LIN PHARMACEUTICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Venice Pharmaceutical Factory Ltd;; Honglin Pharmaceutical Co., Ltd, 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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9614f926daf63c383832457d20799fb4
Registration Details
Taiwan FDA Registration: 9614f926daf63c383832457d20799fb4
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Device Details

"ASTF" cold compress (unsterilized)
TW: "ไบžๅฃซ็‰นๅŠ"ๅ†ทๆ•ท่ฒผ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

9614f926daf63c383832457d20799fb4

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".

o Physical Medical Sciences

O.5700 ้†ซ็™‚็”จๅ†ท็†ฑๆ•ท่ฃ็ฝฎ

Domestic;; Contract manufacturing

Dates and Status

Jan 17, 2018

Jan 17, 2023

Sep 30, 2021

Cancellation Information

Logged out

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