Announcement of GVM2-3.053 Version:
Mirari® Cold Plasma Projection Device

To: Valued Customers, Partners, and All Relevant Individuals and Organizations

Mirari Import-Export Joint Stock Company is pleased to announce:

In order to fully comply with Clause a, Point 2, Article 52 of Decree 98/2021/ND-CP on medical equipment management and to ensure user safety, we officially recommend our partners and customers to only use version GVM2-3.053:

✅ FDA-Safe Version: Mirari® Cold Plasma Projection Device GVM2-3.053

• Manufactured by: General Vibronics Group – USA
• Approved by: U.S. FDA in November 2024
• Meets all international standards for safety and medical effectiveness in wound treatment, pain relief, dermatology, and musculoskeletal care.

Image of the Mirari Cold Plasma Projection Device version GVM2-3.053

⚠️ Warning: Older Devices May Not Be Safe

Mirari Cold Plasma Projection Devices prior to GVM2-3.053:

• Do not meet the quality standards under current FDA regulations.
• Are no longer guaranteed by Mirari Import-Export JSC for quality, effectiveness, or user rights after the upgrade program ends (March 2025).
• Touch arrays of Mirari Cold Plasma devices manufactured before version GVM2-3.053 are incompatible with GVM2-3.053 devices and vice versa.

Images of Mirari Cold Plasma devices from generations prior to GVM2-3.053

🔄 About the Upgrade Program

• From January 2025 to March 2025, Mirari Import-Export JSC implemented an upgrade program for customers using older versions.
• After this period, all non-upgraded devices no longer meet international safety and medical effectiveness standards.

CONTACT INFORMATION

For official product information, please contact:

Mirari JSC – Exclusive Distributor of MIRARI® in Vietnam

Address: 139 Hong Ha, Duc Nhuan Ward, Ho Chi Minh City

Website: https://miraridoctor.vn

Email: contact@miraridoctor.vn

Hotline: 0888 67 06 06

🎯 We sincerely thank our customers and partners for their continued cooperation and support!