Amniotic Fluid - Vietnam Registration 220000821/PCBA-HN
Access comprehensive regulatory information for Amniotic Fluid in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại A medical device is registered under number 220000821/PCBA-HN and manufactured by FUSI Pharmaceutical and Medical Equipment Corporation.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Theo theo phụ lục, QIAGEN Sciences LLC, and 3 recent registrations in the same category. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Technical Details
- Mouthwash solution Medtol with Nano Silver component has antibacterial, antifungal, antiviral effects, eliminates the mouth and throat area, and cleans the mouth and teeth. - It helps prevent and eliminate the harmful bacteria, viruses, and fungi that cause mouth and throat infections, tooth decay, bad breath, and brings a fresh, natural, and gentle breath. - It supports the treatment of cases of pharyngitis, tonsillitis, gingivitis, and other mouth and teeth conditions. - It helps prevent respiratory tract infections such as the common flu, flu A, and hand, foot, and mouth disease in children.
Dates and Status
Mar 08, 2022
AmniSure ROM Test - Qualitative PAMG-1 kit, for detecting amniotic fluid
AmniSure® ROM Test
QIAGEN Sciences LLC
230001580/PCBB-HCM
Amniotic fluid culture with drug
Theo theo phụ lục
180000001/PCBA-TTH
Amniotic fluid culture with drug
Theo theo phụ lục
170000661/PCBA-HN