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Ammora Warm Patch (Unsterilized) - Taiwan Registration 9b3f5ecc6b3ebb06ed0781dee58b20b7

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 9b3f5ecc6b3ebb06ed0781dee58b20b7 and manufactured by HEFEI KOBAYASHI DAILY PRODUCTS 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 SHANGHAI KOBAYASHI DAILY CHEMICALS 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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9b3f5ecc6b3ebb06ed0781dee58b20b7
Registration Details
Taiwan FDA Registration: 9b3f5ecc6b3ebb06ed0781dee58b20b7
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Device Details

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

Registration Details

9b3f5ecc6b3ebb06ed0781dee58b20b7

DHA09600221609

Company Information

Product Details

Limited to the classification and grading management of medical equipment, the first level identification range of "Discardable Hot and Cold Compress Packs for Medical Use (O.5710)".

o Physical Medical Sciences

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

Chinese goods;; input

Dates and Status

Sep 11, 2014

Sep 11, 2029

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