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"Azusa Source" hydrophilic wound litter (sterilization) - Taiwan Registration e8a03684ee257e203545e8d2fa48b3ec

Access comprehensive regulatory information for "Azusa Source" hydrophilic wound litter (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e8a03684ee257e203545e8d2fa48b3ec and manufactured by Oriental Innovation Development Co., Ltd. Biomedical Factory. The authorized representative in Taiwan is Human Origin Biotechnology 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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e8a03684ee257e203545e8d2fa48b3ec
Registration Details
Taiwan FDA Registration: e8a03684ee257e203545e8d2fa48b3ec
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Device Details

"Azusa Source" hydrophilic wound litter (sterilization)
TW: โ€œๆข“ๆบโ€่ฆชๆฐดๆ€งๅ‚ทๅฃๆ•ทๆ–™ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e8a03684ee257e203545e8d2fa48b3ec

Company Information

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound Covering Materials (I.4018)".

I General, Plastic Surgery and Dermatology

I.4018 ่ฆชๆฐดๆ€งๅ‰ตๅ‚ท่ฆ†่“‹ๆ

ๅง”่จ—่ฃฝ้€ ;; ๅœ‹็”ข;; QMS/QSD

Dates and Status

Jul 04, 2012

Jul 04, 2017

Nov 15, 2019

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ