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"BADER" Bright Eye Pad (unsterilized) - Taiwan Registration e45f9db9913578b212697e89c9c5ab61

Access comprehensive regulatory information for "BADER" Bright Eye Pad (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e45f9db9913578b212697e89c9c5ab61 and manufactured by PLASTOD S.P.A.;; Takarajima Eisai Co., Ltd.;; Herui Xingye Co., Ltd. The authorized representative in Taiwan is HOREB ENTERPRISE 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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e45f9db9913578b212697e89c9c5ab61
Registration Details
Taiwan FDA Registration: e45f9db9913578b212697e89c9c5ab61
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Device Details

"BADER" Bright Eye Pad (unsterilized)
TW: "ๆŸๅพท"้ฉๅพ—ๆ˜Ž็œผๅขŠ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

e45f9db9913578b212697e89c9c5ab61

DHA04401271307

Company Information

Product Details

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

I General, Plastic Surgery and Dermatology

I.4440 Eye pads

import

Dates and Status

Feb 19, 2013

Feb 19, 2023