Pure Global

"Ruimei" triple blood cell separator - Taiwan Registration 3e96eac96014db9a71b86084f1b9bae9

Access comprehensive regulatory information for "Ruimei" triple blood cell separator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3e96eac96014db9a71b86084f1b9bae9 and manufactured by REV-MED, Inc.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.

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
3e96eac96014db9a71b86084f1b9bae9
Registration Details
Taiwan FDA Registration: 3e96eac96014db9a71b86084f1b9bae9
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Ruimei" triple blood cell separator
TW: "็‘ž็พŽ" ไธ‰่ฏ่ก€็ƒ็ดฐ่ƒžๅˆ†้›ขๅ™จ
Risk Class 2

Registration Details

3e96eac96014db9a71b86084f1b9bae9

DHA05603439909

Company Information

Korea, Republic of

Product Details

The TriCell PRP Kit is designed to remove blood from patients and centrifuge to prepare Platelet-rich plasma (PRP) for patient use.

B Hematology, pathology, and genetics

B.9245 Automated hemocytoseparator

Input;; QMS/QSD

Dates and Status

Apr 20, 2021

Apr 20, 2026