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"Baoshield" Catheter Fixation Patch (Sterilized) - Taiwan Registration 1a49343992b02f47c4e41411ea32c860

Access comprehensive regulatory information for "Baoshield" Catheter Fixation Patch (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1a49343992b02f47c4e41411ea32c860 and manufactured by PHARMAPLAST S.A.E.. The authorized representative in Taiwan is ASIA HEALTHCARE INC., TAIWAN BRANCH (BVI).

This page provides complete technical specifications, regulatory compliance details. 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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1a49343992b02f47c4e41411ea32c860
Registration Details
Taiwan FDA Registration: 1a49343992b02f47c4e41411ea32c860
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Device Details

"Baoshield" Catheter Fixation Patch (Sterilized)
TW: "ไฟ็›พ" ๅฐŽ็ฎกๅ›บๅฎš่ฒผ็‰‡(ๆป…่Œ)
Risk Class 1

Registration Details

1a49343992b02f47c4e41411ea32c860

DHA09402366908

Company Information

Egypt

Product Details

It is limited to the first level identification scope of the Intravascular Catheter Fixation Device (J.5210) of the Classification and Grading Management Measures for Medical Devices.

J General hospital and personal use equipment

J.5210 ่ก€็ฎกๅ…งๅฐŽ็ฎกๅ›บๅฎš่ฃ็ฝฎ

Input;; QMS/QSD

Dates and Status

Nov 12, 2024

Nov 12, 2029