Vietnam MOH registration 240000618/PCBA-HN

Concentrated Aqueous Solution

VN: DUNG DỊCH XỊT HỌNG
Vietnam flagVietnam·Risk Class TTBYT Loại A·SANFO KEO ONG·SanfordPharma USA, LLC·Registered Apr 19, 2024
Registration details
Analysis ID
240000618/PCBA-HN
Submission ID
000.00.19.H26-240411-0031
Product Type
SANFO KEO ONG
Company information
Manufacturer Country
VIET NAM
Product Owner
CÔNG TY TNHH SANFORDPHARMA USA
Authorized Representative
CÔNG TY TNHH SANFORDPHARMA USA
Technical details
Intended Use
Supports in reducing cough, sore throat, respiratory tract inflammation, dry throat symptoms, throat pain, itchy throat, hoarseness, and difficulty swallowing. Supports in enhancing the immune system, reducing the growth of bacteria, and reducing bad breath.
Dates and status
Registration Date
Apr 19, 2024
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About this record

Access comprehensive regulatory information for Concentrated Aqueous Solution 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 240000618/PCBA-HN and manufactured by SanfordPharma USA, LLC. The authorized representative in Vietnam is CÔNG TY TNHH SANFORDPHARMA USA.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including ICCI Cosmetic Pharmaceutical Corporation, BMP Pharmaceutical Corporation, and 5 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.

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