X-CUBE 90

GUDID 08800013541000

The X-CUBE 90 diagnostic ultrasound system is intended for use by, or by the order of, and under the supervision of, a licensed physician who is qualified for the evaluation of soft tissue and blood flow in the clinical applications of Fetal; Abdominal(renal & GYN/pelvic); Pediatric; Small Organ(breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Trans-rectal; Trans-vaginal; Musculo-skeletal(Conventional); Musculo-skeletal(Superficial); Cardiac(adult& pediatric); Peripheral Vessel(PV); and Urology(including prostate). And, in the imaging modes of 2D(B) mode; Harmonic mode(HAR); M mode; Color M mode; Anatomical M mode; Color Flow Doppler(CF) Mode; Power Doppler(PD) Mode; Directional PD mode; Pulsed Wave Doppler(PWD) Mode; Continuous Wave Doppler(CWD) Mode; High PRF Doppler mode; Tissue Doppler Imaging(TDI) Mode; 3D/4D mode. The X-CUBE 90 is intended to be used in a hospital or medical clinic.

ALPINION MEDICAL SYSTEMS CO.,LTD

General-purpose ultrasound imaging system

• Primary Device ID: 08800013541000
• NIH Device Record Key: 2767c3d0-cfc7-4347-9318-4e47b8225752
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: X-CUBE 90
• Version Model Number: X-CUBE 90
• Company DUNS: 557800655
• Company Name: ALPINION MEDICAL SYSTEMS CO.,LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800013541000 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K200449

FDA Product Code

• ITX: Transducer, Ultrasonic, Diagnostic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-07-23
• Device Publish Date: 2020-07-15

Devices Manufactured by ALPINION MEDICAL SYSTEMS CO.,LTD

• 08800013510037 - L3-12HWD: 2022-11-02
• 08800013510075 - L3-12X: 2022-11-02
• 08800013510150 - L3-8H: 2022-11-02
• 08800013512093 - P1-5CT: 2022-11-02
• 08800013513076 - EC3-10T: 2022-11-02
• 08800013513083 - EV3-10T: 2022-11-02
• 08800013515001 - VE3-10H: 2022-11-02
• 08800013519016 - CW5.0: 2022-11-02