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"Po Ling" Medical Cold Pack (Unsterilized) - Taiwan Registration 04f591ac1b6c9280ee87854e07f8c068

Access comprehensive regulatory information for "Po Ling" Medical Cold Pack (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 04f591ac1b6c9280ee87854e07f8c068 and manufactured by FUSO TEIYAKU QINGDAO CO., LTD.. The authorized representative in Taiwan is PANION & BF BIOTECH INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUSO TEIYAKU QINGDAO 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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04f591ac1b6c9280ee87854e07f8c068
Registration Details
Taiwan FDA Registration: 04f591ac1b6c9280ee87854e07f8c068
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Device Details

"Po Ling" Medical Cold Pack (Unsterilized)
TW: โ€œๅฏถ้ฝกโ€้†ซ็™‚็”จๅ†ทๆ•ทๅŒ… (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

04f591ac1b6c9280ee87854e07f8c068

DHA08600362509

Company Information

Product Details

Limited to the classification and grading management of medical equipment, the first level identification range of "Medical Hot and Cold Compress Device (O.5700)".

o Physical Medical Sciences

O.5700 ้†ซ็™‚็”จๅ†ท็†ฑๆ•ท่ฃ็ฝฎ

Chinese goods;; input

Dates and Status

Oct 01, 2021

Oct 31, 2025

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