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"plusoptiX" Manual Refractor (Non-Sterile) - Taiwan Registration 9dd82b655cd61060897d8864bd2d9b2f

Access comprehensive regulatory information for "plusoptiX" Manual Refractor (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 9dd82b655cd61060897d8864bd2d9b2f and manufactured by PLUSOPTIX GMBH. The authorized representative in Taiwan is EVERVISION INSTRUMENT CO..

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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9dd82b655cd61060897d8864bd2d9b2f
Registration Details
Taiwan FDA Registration: 9dd82b655cd61060897d8864bd2d9b2f
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Device Details

"plusoptiX" Manual Refractor (Non-Sterile)
TW: "ๆ™ฎๅฅงๆๆ–ฏ" ๆ‰‹ๅ‹•ๆŠ˜ๅฐ„่จˆ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

9dd82b655cd61060897d8864bd2d9b2f

Ministry of Health Medical Device Import No. 013335

DHA09401333502

Company Information

Germany

Product Details

M Ophthalmic devices

M1770 Manual Fold Meter

Imported from abroad

Dates and Status

Aug 27, 2013

Aug 27, 2018

Jun 07, 2022

Cancellation Information

Logged out

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