Artificial bone - Vietnam Registration 2403520ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Artificial bone in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại D medical device is registered under number 2403520ĐKLH/BYT-HTTB and manufactured by CG Bio Co., Ltd.. The authorized representative in Vietnam is VĂN PHÒNG ĐẠI DIỆN DAEWOONG PHARMACEUTICAL CO., LTD. TẠI THÀNH PHỐ HỒ CHÍ MINH.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Osteomed, Biomatlante, 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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2403520ĐKLH/BYT-HTTB

Registration Details

Vietnam MOH Registration: 2403520ĐKLH/BYT-HTTB

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Device Details

Artificial bone

VN: Xương nhân tạo

Bongener

Risk Class TTBYT Loại D

Registration Details

Analysis ID

2403520ĐKLH/BYT-HTTB

Submission ID

000.00.04.G18-220629-0039

Product Type

Theo theo phụ lục

Product Code

Theo phụ lục

Technical Details

Intended Use

Bongener is used as a bone graft material for areas of bone deficiency or bone defects that are not related to the stability of the bone structure. It is indicated to fill bone defects and cavities of the skeletal system (such as the limbs, spine, pelvis, etc.), and to fill and/or correct bone defects in the mouth and jaw. These defects may be caused by surgery or bone trauma. The product provides a bone graft material that is capable of reabsorption and is replaced by bone during the healing process.