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"Rheinland" manual eye surgery instruments - Taiwan Registration 0e2ccdc732c4a1661027cfc84f77250c

Access comprehensive regulatory information for "Rheinland" manual eye surgery instruments in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0e2ccdc732c4a1661027cfc84f77250c and manufactured by RHEIN MEDICAL INC.. The authorized representative in Taiwan is FEDERAL MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RHEIN MEDICAL INC., and 1 recent registrations in the same category. 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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0e2ccdc732c4a1661027cfc84f77250c
Registration Details
Taiwan FDA Registration: 0e2ccdc732c4a1661027cfc84f77250c
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Device Details

"Rheinland" manual eye surgery instruments
TW: "่Š่Œต" ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ
Risk Class 1
Cancelled

Registration Details

0e2ccdc732c4a1661027cfc84f77250c

DHA04400423705

Company Information

United States

Product Details

M Ophthalmology

M.4350 ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

import

Dates and Status

Apr 26, 2006

Apr 26, 2011

Nov 26, 2012

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ

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