Pure Global

HỖN DỊCH UỐNG REFLUMAX - Vietnam Registration 240003137/PCBB-HN

Access comprehensive regulatory information for HỖN DỊCH UỐNG REFLUMAX in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TBYT Loại B medical device is registered under number 240003137/PCBB-HN and manufactured by Gruppo Farmaimpresa srl. The authorized representative in Vietnam is CÔNG TY TNHH THƯƠNG MẠI DƯỢC PHẨM PHƯƠNG LINH.

This page provides complete technical specifications, regulatory compliance details. 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.

Free Database
Powered by Pure Global AI
300,000+ Devices
240003137/PCBB-HN
Registration Details
Vietnam MOH Registration: 240003137/PCBB-HN
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

HỖN DỊCH UỐNG REFLUMAX
Risk Class TBYT Loại B

Registration Details

240003137/PCBB-HN

000.00.19.H26-241105-0032

REFLUMAX

Company Information

Gruppo Farmaimpresa srl

Technical Details

REFLUMAX is a medical device that is prescribed to alleviate symptoms of all conditions related to gastroesophageal reflux (heartburn, acid regurgitation, burning sensation in the esophagus, esophagus hypersensitive to acid and non-acid reflux, esophagitis, cough due to acid reflux, abdominal pain).

Dates and Status

Nov 15, 2024