Vietnam MOH registration 240000041/PCBA-VP
Fixed guidewire reinforcement
VN: Gạc cố định kim luồn
Registration details
- Analysis ID
- 240000041/PCBA-VP
- Submission ID
- 000.00.17.H62-240923-0001
- Product Type
- Theo theo phụ lục
- Product Code
- Theo phụ lục
Company information
- Manufacturer
- Công ty Cổ phần Công nghệ Lavitec
- Manufacturer Country
- Theo theo phụ lục
- Product Owner
- Công ty Cổ phần Công nghệ Lavitec
- Authorized Representative
- CÔNG TY CỔ PHẦN CÔNG NGHỆ LAVITEC
Technical details
- Intended Use
- Products used for wound care of patients in hospitals, clinics, health care centers, and laboratories. They are intended to: stabilize and protect catheters, guidewires; stabilize devices used on the skin.
Dates and status
- Registration Date
- Oct 11, 2024
About this record
Access comprehensive regulatory information for Fixed guidewire reinforcement in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TBYT Loại A medical device is registered under number 240000041/PCBA-VP and manufactured by Công ty Cổ phần Công nghệ Lavitec. The authorized representative in Vietnam is CÔNG TY CỔ PHẦN CÔNG NGHỆ LAVITEC.
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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