Taiwan FDA registration ff068b963db7143fac9e6c2784e041e3

"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 Dec 04, 2018 – Dec 04, 2023Cancelled
Registration details
Analysis ID
ff068b963db7143fac9e6c2784e041e3
Customs Code
DHA09600362505
Company information
Manufacturer Country
China
Authorized Representative
PANION & BF BIOTECH INC.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (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
Dec 04, 2018
Expiry Date
Dec 04, 2023
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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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 ff068b963db7143fac9e6c2784e041e3 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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