Vietnam MOH registration 240000833/PCBB-HCM
East Environment / Embryo Dissolution
VN: Môi trường Đông / Rã phôi
Vietnam·Risk Class TTBYT Loại B·Theo theo phụ lục·REPROLIFE Inc.·Registered Apr 19, 2024Registration details
- Analysis ID
- 240000833/PCBB-HCM
- Submission ID
- 000.00.19.H29-240408-0012
- Product Type
- Theo theo phụ lục
- Product Code
- Theo phụ lục
Company information
- Manufacturer
- REPROLIFE Inc.
- Manufacturer Country
- Theo theo phụ lục
- Product Owner
- REPROLIFE Inc.
- Authorized Representative
- CÔNG TY TNHH TOÀN ÁNH
Technical details
- Intended Use
- Used in the process of Embryo/Pre-implantation in Assisted Reproductive Processes
Dates and status
- Registration Date
- Apr 19, 2024
About this record
Access comprehensive regulatory information for East Environment / Embryo Dissolution in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại B medical device is registered under number 240000833/PCBB-HCM and manufactured by REPROLIFE Inc.. The authorized representative in Vietnam is CÔNG TY TNHH TOÀN ÁNH.
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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