Pure Global

Badi Iron D-Dimer Test-Quality Fluid - Taiwan Registration 177d64046c82e5c82c4b44f50dbdd800

Access comprehensive regulatory information for Badi Iron D-Dimer Test-Quality Fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 177d64046c82e5c82c4b44f50dbdd800 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
177d64046c82e5c82c4b44f50dbdd800
Registration Details
Taiwan FDA Registration: 177d64046c82e5c82c4b44f50dbdd800
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Badi Iron D-Dimer Test-Quality Fluid
TW: ๅทด่ฟช้ตๅ…‹ D-ไบŒ่š้ซ”ๆชข้ฉ—่ฉฆๅŠ‘-ๅ“็ฎกๆถฒ
Risk Class 2

Registration Details

177d64046c82e5c82c4b44f50dbdd800

DHA05603752006

Company Information

Korea, Republic of

Product Details

This product is used for quality control of D-dimer testing reagents manufactured/supplied by Boditech Med Inc.

A Clinical chemistry and clinical toxicology

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

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Dec 04, 2024

Dec 04, 2029