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"Dr. Lun" Anshia Eye Surgical Perfusion Device (Sterilized) - Taiwan Registration 94ea36582b7ca9ffd735ce6871aff454

Access comprehensive regulatory information for "Dr. Lun" Anshia Eye Surgical Perfusion Device (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 94ea36582b7ca9ffd735ce6871aff454 and manufactured by BAUSCH & LOMB IRELAND. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

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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94ea36582b7ca9ffd735ce6871aff454
Registration Details
Taiwan FDA Registration: 94ea36582b7ca9ffd735ce6871aff454
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Device Details

"Dr. Lun" Anshia Eye Surgical Perfusion Device (Sterilized)
TW: โ€œๅšๅฃซๅ€ซโ€ ๅฎ‰่ฆ–ไบž็œผ็›ๆ‰‹่ก“็Œๆณจ่ฃ็ฝฎ(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

94ea36582b7ca9ffd735ce6871aff454

DHA04401118006

Company Information

Ireland

Product Details

Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Eye Surgical Perfusion Device (M.4360)".

M Ophthalmology

M.4360 Perfusion device for ophthalmic surgery

Input;; QMS/QSD

Dates and Status

Dec 14, 2011

Dec 14, 2016

Apr 25, 2018

Cancellation Information

Logged out

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