Taiwan FDA registration 4cf00b59743825bdf4e77e406f8f14d3

"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 24, 2006 – Apr 24, 2026Expired
Registration details
Analysis ID
4cf00b59743825bdf4e77e406f8f14d3
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-motive, single patient-use, carry-on suctioning device
Import Information
國產;; QMS/QSD
Dates and status
Registration Date
Apr 24, 2006
Expiry Date
Apr 24, 2026
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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 4cf00b59743825bdf4e77e406f8f14d3 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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