Vietnam MOH registration 240000050/PCBA-LA
Fibrinolytic Enzyme
VN: DẦU CẦM MÁU
Registration details
- Analysis ID
- 240000050/PCBA-LA
- Submission ID
- 000.00.17.H39-240513-0007
- Product Type
- DCM
Company information
- Manufacturer
- CÔNG TY CỔ PHẦN DI HÀO
- Manufacturer Country
- VIET NAM
- Product Owner
- CÔNG TY CỔ PHẦN DI HÀO
- Authorized Representative
- CÔNG TY CỔ PHẦN DI HÀO
Technical details
- Intended Use
- Topical product used for external application, to relieve pain and discomfort caused by injuries, back pain, muscle tension, cramps, numbness, and to help reduce bruising and swelling,...
Dates and status
- Registration Date
- May 23, 2024
About this record
Access comprehensive regulatory information for Fibrinolytic Enzyme in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại A medical device is registered under number 240000050/PCBA-LA and manufactured by CÔNG TY CỔ PHẦN DI HÀO. The authorized representative in Vietnam is CÔNG TY CỔ PHẦN DI HÀO.
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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