KONQUEST

GUDID 00850021777005

FINGERTIP PULSE OXIMENTER

KONQUEST GROUP INC

Pulse oximeter, battery-powered

• Primary Device ID: 00850021777005
• NIH Device Record Key: a29b4bff-6465-434c-b085-a447c1465324
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KONQUEST
• Version Model Number: KPO-1720
• Company DUNS: 080939375
• Company Name: KONQUEST GROUP INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: false
• 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	00850021777005 [Primary]

FDA Product Code

• OCH: Oximeter, Infrared, Sporting, Aviation

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: 2020-09-09
• Device Publish Date: 2020-09-01

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