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Treatment Grid for Partial Spontaneous Evisceration - Vietnam Registration 2402094ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Treatment Grid for Partial Spontaneous Evisceration in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại C medical device is registered under number 2402094ĐKLH/BYT-HTTB and manufactured by Johnson & Johnson International. The authorized representative in Vietnam is CÔNG TY TNHH JOHNSON & JOHNSON (VIỆT NAM).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Theo theo phụ lục, and 1 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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2402094ĐKLH/BYT-HTTB
Registration Details
Vietnam MOH Registration: 2402094ĐKLH/BYT-HTTB
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Device Details

Treatment Grid for Partial Spontaneous Evisceration
VN: Lưới điều trị thoát vị tự tiêu một phần
Risk Class TTBYT Loại C

Registration Details

2402094ĐKLH/BYT-HTTB

17004709/ĐKLH-BYT-TB-CT

Theo theo phụ lục

Theo phụ lục

Company Information

Theo theo phụ lục

Johnson & Johnson International

Technical Details

The ULTRAPRO ADVANCED Mesh is indicated for the repair of abdominal hernia and abdominal wall defects that require additional reinforcement material to achieve the desired surgical outcome.

Dates and Status

Aug 27, 2024

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