Pure Global

Sigu Blood Cell Separator - Taiwan Registration 12a1fe999411cd47104febb0fe1995d6

Access comprehensive regulatory information for Sigu Blood Cell Separator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 12a1fe999411cd47104febb0fe1995d6 and manufactured by BIOSAFE Ltd. The authorized representative in Taiwan is QUALTECH CONSULTING 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
12a1fe999411cd47104febb0fe1995d6
Registration Details
Taiwan FDA Registration: 12a1fe999411cd47104febb0fe1995d6
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Sigu Blood Cell Separator
TW: ๆ€ๆฒ›ๅ…‹่ก€็ƒ็ดฐ่ƒžๅˆ†้›ขๆฉŸ
Risk Class 3

Registration Details

12a1fe999411cd47104febb0fe1995d6

DHA00602414505

Company Information

Switzerland

Product Details

For details, it is Chinese approved copy of the imitation order

B Hematology, pathology, and genetics

B.9245 Automated hemocytoseparator

import

Dates and Status

Oct 26, 2012

Oct 26, 2027