Taiwan FDA registration 04f591ac1b6c9280ee87854e07f8c068

"Po Ling" Medical Cold Pack (Unsterilized)

TW: “寶齡”醫療用冷敷包 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·FUSO TEIYAKU QINGDAO CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
04f591ac1b6c9280ee87854e07f8c068
Customs Code
DHA08600362509
Company information
Manufacturer Country
China
Authorized Representative
PANION & BF BIOTECH INC.
Product details
Intended Use
Limited to the classification and grading management of medical equipment, the first level identification range of "Medical Hot and Cold Compress Device (O.5700)".
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.5700 醫療用冷熱敷裝置
Import Information
Chinese goods;; input
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

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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