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Sanmeng corrected reference serum - Taiwan Registration 584b49d0685f29d05ccab2ede0a11158

Access comprehensive regulatory information for Sanmeng corrected reference serum in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 584b49d0685f29d05ccab2ede0a11158 and manufactured by THERMO ELECTRON CORPORATION. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A SUBSIDIARY OF THERMO FISHER, and 1 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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584b49d0685f29d05ccab2ede0a11158
Registration Details
Taiwan FDA Registration: 584b49d0685f29d05ccab2ede0a11158
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Device Details

Sanmeng corrected reference serum
TW: ไธ‰็›Ÿ ๆ กๆญฃๅƒ่€ƒ่ก€ๆธ…
Risk Class 2
Cancelled

Registration Details

584b49d0685f29d05ccab2ede0a11158

DHA00601633004

Company Information

Australia

Product Details

It is used for the second correction on the clinical chemical analysis instrument.

A Clinical chemistry and clinical toxicology

A.1150 Calibrated Products

import

Dates and Status

Apr 11, 2006

Apr 11, 2011

Oct 29, 2012

Cancellation Information

Logged out

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