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"REDA" Eye Pad (Non-Sterile) - Taiwan Registration cfe9e42ea7e1875b924fb440f977bc7a

Access comprehensive regulatory information for "REDA" Eye Pad (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 cfe9e42ea7e1875b924fb440f977bc7a and manufactured by REDA INSTRUMENTE (ASIA -PACIFIC) PTE LTD. The authorized representative in Taiwan is Medical Dragon 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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cfe9e42ea7e1875b924fb440f977bc7a
Registration Details
Taiwan FDA Registration: cfe9e42ea7e1875b924fb440f977bc7a
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Device Details

"REDA" Eye Pad (Non-Sterile)
TW: "้ณ้ฝ" ่ญท็œผ่ฒผ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

cfe9e42ea7e1875b924fb440f977bc7a

Ministry of Health Medical Device Import No. 020450

DHA09402045003

Company Information

Product Details

Limited to the first level recognition range of eye pads (I.4440) of the medical equipment management method.

I General and plastic surgical devices

I4440 Eye pads

Imported from abroad

Dates and Status

May 16, 2019

May 16, 2024