Pure Global

"Beckman Coulter" DxH 500 Series Hemolytic Agents (Uninbacteric) - Taiwan Registration b99d6cf07c679036f9a5122d91ac1fda

Access comprehensive regulatory information for "Beckman Coulter" DxH 500 Series Hemolytic Agents (Uninbacteric) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b99d6cf07c679036f9a5122d91ac1fda and manufactured by BIT GROUP FRANCE;; BECKMAN COULTER IRELAND INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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
b99d6cf07c679036f9a5122d91ac1fda
Registration Details
Taiwan FDA Registration: b99d6cf07c679036f9a5122d91ac1fda
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Beckman Coulter" DxH 500 Series Hemolytic Agents (Uninbacteric)
TW: "่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰น" DxH 500 ็ณปๅˆ—่ก€็ƒๆบถ่ก€ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

b99d6cf07c679036f9a5122d91ac1fda

DHA09402368608

Company Information

Product Details

It is limited to the first-level identification scope of the "Erythrolytic Agents (B.8540)" of the Administrative Measures for the Classification and Grading of Medical Devices.

B Hematology, pathology, and genetics

B.8540 ็ด…่ก€็ƒๆบถ่งฃๅŠ‘

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Nov 22, 2024

Nov 22, 2029