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Badi Tieke High Sensitivity C-Reactive Protein Quality Tube - Taiwan Registration 5e524144c882b901d21d80a7bacc1538

Access comprehensive regulatory information for Badi Tieke High Sensitivity C-Reactive Protein Quality Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5e524144c882b901d21d80a7bacc1538 and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is MEDRICH INSTRUMENT 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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5e524144c882b901d21d80a7bacc1538
Registration Details
Taiwan FDA Registration: 5e524144c882b901d21d80a7bacc1538
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Device Details

Badi Tieke High Sensitivity C-Reactive Protein Quality Tube
TW: ๅทด่ฟช้ตๅ…‹้ซ˜้ˆๆ•ๆ€ง C ๅๆ‡‰่›‹็™ฝๅ“็ฎกๆถฒ
Risk Class 2

Registration Details

5e524144c882b901d21d80a7bacc1538

DHA05603706508

Company Information

Korea, Republic of

Product Details

This product is used for quality control of highly sensitive C-reactive protein assays manufactured and supplied by Boditech.

A Clinical chemistry and clinical toxicology

A.1660 Quality control materials (analytical and non-analytical)

Input;; QMS/QSD

Dates and Status

Mar 04, 2024

Mar 04, 2029