Product - Vietnam Registration 240000002/PCBB-AG

Access comprehensive regulatory information for Product 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 240000002/PCBB-AG and manufactured by CPC1 Pharmaceutical Corporation, Hanoi. The authorized representative in Vietnam is ĐỊA ĐIỂM KINH DOANH - CÔNG TY CỔ PHẦN UPHARMA - NHÀ THUỐC UPHARMA SỐ 72.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including MetaSystems Probes GmbH, Bio-Rad, 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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240000002/PCBB-AG

Registration Details

Vietnam MOH Registration: 240000002/PCBB-AG

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Device Details

Product

VN: Sản phẩm

Gravia sup 200 mg

Risk Class TBYT Loại B

Registration Details

Analysis ID

240000002/PCBB-AG

Submission ID

000.00.15.H01-240930-0002

Product Type

TCCS-45B:2022/CPC1HN

Technical Details

Intended Use

It helps to treat cases of vaginal and vulvar candidiasis (usually caused by Candida albicans), trichomoniasis, or other infections sensitive to Clotrimazol, as evidenced by the following symptoms: vaginal and vulvar redness, swelling, burning sensation during urination or sexual intercourse, and white, cheese-like vaginal discharge. The suppository is intended for use in adults and children aged 12 and above.