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"Heidelberg" retinal tomography - Taiwan Registration 7b0b2676d95c7f58d2cbc7f29bf7153d

Access comprehensive regulatory information for "Heidelberg" retinal tomography in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7b0b2676d95c7f58d2cbc7f29bf7153d and manufactured by HEIDELBERG ENGINEERING GMBH. The authorized representative in Taiwan is CLINICO INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HEIDELBERG ENGINEERING GMBH, and 2 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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7b0b2676d95c7f58d2cbc7f29bf7153d
Registration Details
Taiwan FDA Registration: 7b0b2676d95c7f58d2cbc7f29bf7153d
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Device Details

"Heidelberg" retinal tomography
TW: โ€œๆตทๅพทๅ กโ€่ฆ–็ถฒ่†œๆ–ทๅฑคๆŽƒ็ž„ๅ„€
Risk Class 2
Cancelled

Registration Details

7b0b2676d95c7f58d2cbc7f29bf7153d

DHA00601834208

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

import

Dates and Status

Sep 29, 2007

Sep 29, 2012

Apr 30, 2014

Cancellation Information

Logged out

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