Treatment Grid for Partial Spontaneous Evisceration
- Analysis ID
- 2402094ĐKLH/BYT-HTTB
- Submission ID
- 17004709/ĐKLH-BYT-TB-CT
- Product Type
- Theo theo phụ lục
- Product Code
- Theo phụ lục
- Manufacturer
- Johnson & Johnson International
- Manufacturer Country
- Theo theo phụ lục
- Product Owner
- Johnson & Johnson International
- Authorized Representative
- CÔNG TY TNHH JOHNSON & JOHNSON (VIỆT NAM)
- Intended Use
- 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.
- Registration Date
- Aug 27, 2024
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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.