NITTOBO LDH (Non-Sterile) - Taiwan Registration eed89a1f61aea454db562be0ce095a64
Access comprehensive regulatory information for NITTOBO LDH (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number eed89a1f61aea454db562be0ce095a64 and manufactured by NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER. The authorized representative in Taiwan is TUNYEN ENTERPRISE 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.
Device Details
Registration Details
eed89a1f61aea454db562be0ce095a64
Ministry of Health Medical Device Import No. 020691
DHA09402069102
Product Details
Limited to the first level recognition range of lactate dehydrogenase test system (A.1440) of the management method for medical devices.
A Clinical chemistry and clinical toxicology
A1440 Lactate dehydrogenase test system
Imported from abroad
Dates and Status
Jul 29, 2019
Jul 29, 2024