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"Heini" fiber optic ophthalmic projector (unsterilized) - Taiwan Registration 094d7bcc1e12af3c49acfbbfe3a5bdd8

Access comprehensive regulatory information for "Heini" fiber optic ophthalmic projector (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 094d7bcc1e12af3c49acfbbfe3a5bdd8 and manufactured by HEINE OPTOTECHNIK GMBH & CO. LTD.. The authorized representative in Taiwan is Poussen Industrial 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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094d7bcc1e12af3c49acfbbfe3a5bdd8
Registration Details
Taiwan FDA Registration: 094d7bcc1e12af3c49acfbbfe3a5bdd8
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Device Details

"Heini" fiber optic ophthalmic projector (unsterilized)
TW: โ€œๆตทๅฐผโ€ๅ…‰็บ–็œผ็ง‘็”จๆŠ•ๅฝฑๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

094d7bcc1e12af3c49acfbbfe3a5bdd8

DHA04400598500

Company Information

Product Details

Limited to the first level recognition range of ophthalmic projectors (M.1680) for the management of medical equipment.

M Ophthalmology

M.1680 ็œผ็ง‘็”จๆŠ•ๅฝฑๆฉŸ

import

Dates and Status

Jul 06, 2007

Jul 06, 2012

May 05, 2014

Cancellation Information

Logged out

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