KONQUEST

GUDID 00850021777043

AUTOMATIC UPPER ARM BLOOD PRESSURE MONITOR

KONQUEST GROUP INC

Blood pressure cuff, reusable

• Primary Device ID: 00850021777043
• NIH Device Record Key: 81deea2d-4fc8-4d81-947a-a39902dee9d5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KONQUEST
• Version Model Number: KBP-7173A
• Company DUNS: 080939375
• Company Name: KONQUEST GROUP INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• 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	00850021777043 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K222125

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive

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: 2023-04-03
• Device Publish Date: 2023-03-24

On-Brand Devices [KONQUEST]

• 00869378000445: DIGITAL WRIST BLOOD PRESSURE MONITOR
• 00869378000438: DIGITAL ARM BLOOD PRESSURE MONITOR
• 00869378000421: Forehead and Ear Infrared Thermometer - Upgraded Firmware
• 00869378000414: DIGITAL FOREHEAD AND EAR IR THERMOMETER
• 00869378000407: DIGITAL BASAL THERMOMETER
• 00850021777005: FINGERTIP PULSE OXIMENTER
• 00850021777036: REPLACEMENT CUFF FOR BLOOD PRESSURE MONITOR
• 00850021777029: REPLACEMENT CUFF FOR BLOOD PRESSURE MONITOR
• 00850021777012: REPLACEMENT CUFF FOR BLOOD PRESSURE MONITOR
• 00850021777043: AUTOMATIC UPPER ARM BLOOD PRESSURE MONITOR