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"Hurricane" Medical absorbent fiber(Non-Sterile) - Taiwan Registration 2526b734bdc977bd0b7b9f7e074adb53

Access comprehensive regulatory information for "Hurricane" Medical absorbent fiber(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2526b734bdc977bd0b7b9f7e074adb53 and manufactured by HURRICANE MEDICAL. 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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2526b734bdc977bd0b7b9f7e074adb53
Registration Details
Taiwan FDA Registration: 2526b734bdc977bd0b7b9f7e074adb53
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Device Details

"Hurricane" Medical absorbent fiber(Non-Sterile)
TW: "่ณ€้†ซ่‚ฏ" ้†ซ็™‚็”จๅธๆ”ถ็บ–็ถญ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2526b734bdc977bd0b7b9f7e074adb53

Ministry of Health Medical Device Import No. 018801

DHA09401880101

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

J5300 Medical Absorbent Fiber

Imported from abroad

Dates and Status

Feb 08, 2018

Feb 08, 2028