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Ammora Warm Patch (Unsterilized) - Taiwan Registration a6230364dae34509c2c51cb43be5ef99

Access comprehensive regulatory information for Ammora Warm Patch (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a6230364dae34509c2c51cb43be5ef99 and manufactured by SHANGHAI KOBAYASHI DAILY CHEMICALS CO., LTD.. The authorized representative in Taiwan is KOBAYASHI PHARMACEUTICAL (TAIWAN) CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HEFEI KOBAYASHI DAILY PRODUCTS 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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a6230364dae34509c2c51cb43be5ef99
Registration Details
Taiwan FDA Registration: a6230364dae34509c2c51cb43be5ef99
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Device Details

Ammora Warm Patch (Unsterilized)
TW: ๅฎ‰ๆ‘ฉๆจ‚ ๆบซ็†ฑๆ•ท่ฒผ็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

a6230364dae34509c2c51cb43be5ef99

DHA04600189100

Company Information

Product Details

It is limited to the first level of identification of the medical equipment management measures "disposable hot and cold compress packs for medical use (O5710)".

o Physical Medical Sciences

O.5710 ้†ซ็™‚็”จๅฏไธŸๆฃ„ๅผ็š„ๅ†ท็†ฑๆ•ทๅŒ…

Chinese goods;; input

Dates and Status

May 14, 2013

May 14, 2018

Nov 04, 2019

Cancellation Information

Logged out

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