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"Akiyama" suture needle for medical treatment (unsterilized) - Taiwan Registration d1e962b381fb34ad45c4a217e891c628

Access comprehensive regulatory information for "Akiyama" suture needle for medical treatment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d1e962b381fb34ad45c4a217e891c628 and manufactured by AKIYAMA MEDICAL MFG. CO. LTD.. The authorized representative in Taiwan is Yingheng Enterprises Limited.

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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d1e962b381fb34ad45c4a217e891c628
Registration Details
Taiwan FDA Registration: d1e962b381fb34ad45c4a217e891c628
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Device Details

"Akiyama" suture needle for medical treatment (unsterilized)
TW: "็ง‹ๅฑฑ"้†ซ็™‚็”จ็ธซๅˆ้‡ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

d1e962b381fb34ad45c4a217e891c628

DHA04400140103

Company Information

Product Details

It is a non-powered, hand-held or hand-operated device that can be reused or thrown away after use, and is used for various general surgeries.

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

import

Dates and Status

Oct 28, 2005

Oct 28, 2025