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"He Yiken" medical absorbent fiber (unsterilized) - Taiwan Registration 0467d1fea83e5bf850d5a7c3cfafa104

Access comprehensive regulatory information for "He Yiken" medical absorbent fiber (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0467d1fea83e5bf850d5a7c3cfafa104 and manufactured by HURRICANE MEDICAL INC.. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..

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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0467d1fea83e5bf850d5a7c3cfafa104
Registration Details
Taiwan FDA Registration: 0467d1fea83e5bf850d5a7c3cfafa104
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Device Details

"He Yiken" medical absorbent fiber (unsterilized)
TW: "่ณ€้†ซ่‚ฏ" ้†ซ็™‚็”จๅธๆ”ถ็บ–็ถญ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0467d1fea83e5bf850d5a7c3cfafa104

DHA04400689004

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Medical Absorbent Fiber (J.5300)".

J General hospital and personal use equipment

J.5300 ้†ซ็™‚็”จๅธๆ”ถ็บ–็ถญ

import

Dates and Status

Jul 09, 2008

Jul 09, 2018

Jun 22, 2022

Cancellation Information

Logged out

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