Taiwan FDA registration ff562ffccdc346fe9285b71e479b0922

"Pacific" closed vacuum wound drainage sleeve (sterilized)

TW: “太平洋”密閉式真空傷口引流套(滅菌)
Taiwan flagTaiwan·Risk Class 1·Pacific Medical Materials Co., Ltd. Copper Factory·Registered Apr 16, 2014 – Apr 16, 2029Active
Registration details
Analysis ID
ff562ffccdc346fe9285b71e479b0922
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
PACIFIC HOSPITAL SUPPLY CO., LTD.
Product details
Intended Use
It is limited to the first level of identification scope of the "Non-powered, Single-Patient Use, Portable Suction Devices (I.4680)" and "Introduction/Drainage Catheters and Their Accessories (I.4200)" in the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4680 Non-motorized, single-patient, carry-on aspiration apparatus; I.4200 Incoming/Drainage Tubes and Accessories
Import Information
QMS/QSD;; 國產
Dates and status
Registration Date
Apr 16, 2014
Expiry Date
Apr 16, 2029
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About this record

Access comprehensive regulatory information for "Pacific" closed vacuum wound drainage sleeve (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ff562ffccdc346fe9285b71e479b0922 and manufactured by Pacific Medical Materials Co., Ltd. Copper Factory. The authorized representative in Taiwan is PACIFIC HOSPITAL SUPPLY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Pacific Medical Materials Co., Ltd. Copper Factory, 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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