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"Venice" cold compress (unsterilized) - Taiwan Registration 9f1ffcf90ee1e514b381e0f725c01e2b

Access comprehensive regulatory information for "Venice" 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 9f1ffcf90ee1e514b381e0f725c01e2b and manufactured by VENICE LABORATORIES CO., LTD.. The authorized representative in Taiwan is VENICE LABORATORIES CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including VENICE LABORATORIES 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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9f1ffcf90ee1e514b381e0f725c01e2b
Registration Details
Taiwan FDA Registration: 9f1ffcf90ee1e514b381e0f725c01e2b
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Device Details

"Venice" cold compress (unsterilized)
TW: โ€œๅจๅฐผๆ–ฏโ€ๅ†ทๆ•ท่ฒผ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

9f1ffcf90ee1e514b381e0f725c01e2b

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

Dates and Status

Jun 02, 2008

Jun 02, 2023

Sep 30, 2021

Cancellation Information

Logged out

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