Pure Global

"TERUMO" CDI HEMATOCRIT/SATURATIN CUVETTE - Taiwan Registration 0b75ed6381dc472e9667077dc3036e15

Access comprehensive regulatory information for "TERUMO" CDI HEMATOCRIT/SATURATIN CUVETTE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0b75ed6381dc472e9667077dc3036e15 and manufactured by TERUMO CARDIOVASCULAR SYSTEMS CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL 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
0b75ed6381dc472e9667077dc3036e15
Registration Details
Taiwan FDA Registration: 0b75ed6381dc472e9667077dc3036e15
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"TERUMO" CDI HEMATOCRIT/SATURATIN CUVETTE
TW: ่ก€ๆฐงๆ„Ÿ็Ÿฅๅ™จ
Risk Class 2
MD

Registration Details

0b75ed6381dc472e9667077dc3036e15

Department of Health Medical Device Import No. 009298

DHA00600929804

Company Information

Product Details

1399 Other blood transfusion, infusion equipment

Imported from abroad

Dates and Status

Sep 10, 1999

Feb 09, 2029