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"Lake" corneal mapper (unsterilized) - Taiwan Registration 6696aab0a2c3494f83bd34abfa06e20e

Access comprehensive regulatory information for "Lake" corneal mapper (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6696aab0a2c3494f83bd34abfa06e20e and manufactured by REICHERT, INC.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.

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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6696aab0a2c3494f83bd34abfa06e20e
Registration Details
Taiwan FDA Registration: 6696aab0a2c3494f83bd34abfa06e20e
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Device Details

"Lake" corneal mapper (unsterilized)
TW: โ€œ่Šๅ…‹โ€่ง’่†œๅœฐๅœ–ๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

6696aab0a2c3494f83bd34abfa06e20e

DHA04400483502

Company Information

United States

Product Details

Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.

M Ophthalmology

M.1350 Coratoscope

import

Dates and Status

Jun 30, 2006

Jun 30, 2011

Nov 27, 2012

Cancellation Information

Logged out

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