AP01 AND AP02

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

GRX Medical

FDA UDI

CARDICARE COMPANY LTD·06970366970085·

ReBOSSIS

FDA registration

Kaigen Pharma Co., Ltd. Tenjin Factory·1 product·🇯🇵 Japan

POLYMER ENGINEERING LABORATORIES LTD.

FDA registration

POLYMER ENGINEERING LABORATORIES LTD.·1 product·🇯🇵 Japan

UNISIS CORP

FDA registration

UNISIS CORP·1 product·🇯🇵 Japan

UNISIS CORP

FDA registration

UNISIS CORP·1 product·🇯🇵 Japan

UNISIS CORP

FDA registration

UNISIS CORP·1 product·🇯🇵 Japan

UNISIS CORP

FDA registration

UNISIS CORP·1 product·🇯🇵 Japan

UNISIS CORP

FDA registration

UNISIS CORP·1 product·🇯🇵 Japan

UNISIS CORP

FDA registration

UNISIS CORP·1 product·🇯🇵 Japan

UNISIS CORP

FDA registration

UNISIS CORP·1 product·🇯🇵 Japan

ReBOSSIS QDS

FDA registration

Kaigen Pharma Co., Ltd. Tenjin Factory·1 product·🇯🇵 Japan

Uniever Disposable Nerve Blockade Needle

FDA registration

UNISIS CORP·1 product·🇯🇵 Japan

UNISIS CORP

FDA registration

UNISIS CORP·1 product·🇯🇵 Japan

Uniever Disposable Spinal Anesthesia Needle

FDA registration

UNISIS CORP·1 product·🇯🇵 Japan

REBOSSIS

FDA registration

Kaigen Pharma Co., Ltd. Tenjin Factory·1 product·🇯🇵 Japan

UNISIS CORP

FDA registration

UNISIS CORP·1 product·🇯🇵 Japan

ReBOSSIS QDS

FDA registration

Kaigen Pharma Co., Ltd. Tenjin Factory·1 product·🇯🇵 Japan

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·VENTRITEX SPL LEAD SYSTEM

PORTRAIT SpO2 P-SP01

FDA UDI

GE Healthcare Finland Oy·00195278264794·PORTRAIT SpO2 P-SP FINAL DEVICE ASSEMBLY