Taiwan FDA registration f42e8120f7337f9b0cd6628b65484803

"Eurowood" Medical Cold Pack (Unsterilized)

TW: “歐活”醫療用冷敷包 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·The second factory of Biao Shi Medical Technology Co., Ltd·Registered Aug 18, 2006 – Aug 18, 2026Cancelled
Registration details
Analysis ID
f42e8120f7337f9b0cd6628b65484803
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
OPPO MEDICAL CORP.
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
Contract manufacturing;; Domestic
Dates and status
Registration Date
Aug 18, 2006
Expiry Date
Aug 18, 2026
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 "Eurowood" 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 f42e8120f7337f9b0cd6628b65484803 and manufactured by The second factory of Biao Shi Medical Technology Co., Ltd. The authorized representative in Taiwan is OPPO MEDICAL CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Oper Co., Ltd.;; The second plant of Biaoshi Medical Technology 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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