Dynarex Protech 45-Day Bed Sensor Pad, 10" x 28"

GUDID 00840117323131

DYNAREX CORPORATION

Bed/chair occupant movement sensor Bed/chair occupant movement sensor Bed/chair occupant movement sensor Bed/chair occupant movement sensor Bed/chair occupant movement sensor Bed/chair occupant movement sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor Bed/chair occupant movement pressure/vibration sensor

• Primary Device ID: 00840117323131
• NIH Device Record Key: 5bb896fe-5f15-4c47-937e-8ff9abd4edd3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dynarex Protech 45-Day Bed Sensor Pad, 10" x 28"
• Version Model Number: P-105497
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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	00840117323124 [Package]; Package: Case [10 Units]; In Commercial Distribution
GS1	00840117323131 [Primary]

FDA Product Code

• KMI: Monitor, Bed Patient

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: 2022-05-31
• Device Publish Date: 2022-05-23

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