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Lendo corrected serum - Taiwan Registration b130d8f956d7579a14c116f9c8420b29

Access comprehensive regulatory information for Lendo corrected serum in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b130d8f956d7579a14c116f9c8420b29 and manufactured by RANDOX LABORATORIES LTD. The authorized representative in Taiwan is EUGENE-CHEN 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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b130d8f956d7579a14c116f9c8420b29
Registration Details
Taiwan FDA Registration: b130d8f956d7579a14c116f9c8420b29
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Device Details

Lendo corrected serum
TW: ๅ€ซๅคšๆ กๆญฃ่ก€ๆธ…
Risk Class 2
Cancelled

Registration Details

b130d8f956d7579a14c116f9c8420b29

DHA00601600802

Company Information

United Kingdom

Product Details

It is used as a corrector in clinical biochemical analysis.

A Clinical chemistry and clinical toxicology

A.1150 Calibrated Products

import

Dates and Status

Feb 17, 2006

Feb 17, 2011

Oct 13, 2011

Cancellation Information

Logged out

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