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AQUA XỊT TRĨ HEMO CARE - Vietnam Registration 240001121/PCBA-HN

Access comprehensive regulatory information for AQUA XỊT TRĨ HEMO CARE 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 240001121/PCBA-HN and manufactured by Syntech Pharmaceutical Co., Ltd. Branch – Hai Phong Factory. The authorized representative in Vietnam is CÔNG TY CỔ PHẦN LIÊN DOANH DƯỢC PHẨM AQUA.

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.

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240001121/PCBA-HN
Registration Details
Vietnam MOH Registration: 240001121/PCBA-HN
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Device Details

AQUA XỊT TRĨ HEMO CARE
VN: AQUA XỊT TRĨ HEMO CARE
Risk Class TTBYT Loại A

Registration Details

240001121/PCBA-HN

000.00.19.H26-240607-0023

HEMO CARE

Company Information

Công ty cổ phần liên doanh Dược phẩm AQUA

Technical Details

- Softening, soothing, and supporting relief of symptoms: swelling, pain, burning, itching, and discomfort due to external hemorrhoids, internal hemorrhoids, mixed hemorrhoids, and chronic constipation. - Supporting the healing of the anal mucosa, thereby reducing the process of hemorrhoid prolapse

Dates and Status

Jun 10, 2024