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"Diener" Manual Eye Surgery Instruments (Unsterilized) - Taiwan Registration 8222b5df51ec5942d3d5b05a637431e3

Access comprehensive regulatory information for "Diener" Manual Eye Surgery Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8222b5df51ec5942d3d5b05a637431e3 and manufactured by CHR. DIENER GMBH & CO. KG. The authorized representative in Taiwan is BIOMEGA INSTRUMENT 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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8222b5df51ec5942d3d5b05a637431e3
Registration Details
Taiwan FDA Registration: 8222b5df51ec5942d3d5b05a637431e3
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Device Details

"Diener" Manual Eye Surgery Instruments (Unsterilized)
TW: โ€œ่ฟช็ดโ€ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

8222b5df51ec5942d3d5b05a637431e3

DHA04400753808

Company Information

Germany

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".

M Ophthalmology

M.4350 ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

import

Dates and Status

Mar 05, 2009

Mar 05, 2014

Jan 09, 2017

Cancellation Information

Logged out

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