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"Heini" retinal scope and its accessories (unsterilized) - Taiwan Registration 847777028dce5bcb61a49fe18a73f6f3

Access comprehensive regulatory information for "Heini" retinal scope and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 847777028dce5bcb61a49fe18a73f6f3 and manufactured by HEINE OPTOTECHNIK GMBH & CO. LTD.. The authorized representative in Taiwan is Meidcheng 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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847777028dce5bcb61a49fe18a73f6f3
Registration Details
Taiwan FDA Registration: 847777028dce5bcb61a49fe18a73f6f3
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Device Details

"Heini" retinal scope and its accessories (unsterilized)
TW: "ๆตทๅฐผ" ่ฆ–็ถฒ่†œ้กๅŠๅ…ถ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

847777028dce5bcb61a49fe18a73f6f3

DHA04400427003

Company Information

Product Details

M Ophthalmology

M.1780 Retinal Lens

import

Dates and Status

Apr 28, 2006

Apr 28, 2011

Aug 18, 2006

Cancellation Information

Logged out

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