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"Virtue Heart" intraocular lens guide (sterilization) - Taiwan Registration b0651df20feccda37e505b3a81aca8db

Access comprehensive regulatory information for "Virtue Heart" intraocular lens guide (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b0651df20feccda37e505b3a81aca8db and manufactured by ROBUTEC AG;; MEDICEL AG. The authorized representative in Taiwan is UNITED MEDICAL INC..

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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b0651df20feccda37e505b3a81aca8db
Registration Details
Taiwan FDA Registration: b0651df20feccda37e505b3a81aca8db
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Device Details

"Virtue Heart" intraocular lens guide (sterilization)
TW: โ€œ็พŽๅพทๅฟƒโ€ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ๏ผˆๆป…่Œ๏ผ‰
Risk Class 1

Registration Details

b0651df20feccda37e505b3a81aca8db

DHA09401337501

Company Information

Switzerland

Product Details

Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.

M Ophthalmology

M.4300 Artificial crystal body inducer

QMS/QSD;; ่ผธๅ…ฅ;; ๅง”่จ—่ฃฝ้€ 

Dates and Status

Sep 04, 2013

Sep 04, 2028