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"Lake" tonometer / corneal thickness measuring instrument - Taiwan Registration 6fc20a002991a2c3635251a0ae13e7b2

Access comprehensive regulatory information for "Lake" tonometer / corneal thickness measuring instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6fc20a002991a2c3635251a0ae13e7b2 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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6fc20a002991a2c3635251a0ae13e7b2
Registration Details
Taiwan FDA Registration: 6fc20a002991a2c3635251a0ae13e7b2
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Device Details

"Lake" tonometer / corneal thickness measuring instrument
TW: โ€œ่Šๅ…‹โ€็œผๅฃ“่จˆ/่ง’่†œๅŽšๅบฆๆธฌ้‡ๅ„€
Risk Class 2
Cancelled

Registration Details

6fc20a002991a2c3635251a0ae13e7b2

DHA00601805301

Company Information

United States

Product Details

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

P Radiology Science

P.1560 ่ถ…้Ÿณๆณขๅ›ž้Ÿณๅฝฑๅƒ็ณป็ตฑ

import

Dates and Status

May 03, 2007

May 03, 2017

Dec 20, 2019

Cancellation Information

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