Air Mattress, Dial Operated Pump, w/Bubble Pad

GUDID 00616784044018

DYNAREX CORPORATION

Alternating-pressure bed mattress overlay system

• Primary Device ID: 00616784044018
• NIH Device Record Key: 5e6a6a3f-63e7-425a-9572-d619f6cd977e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Air Mattress, Dial Operated Pump, w/Bubble Pad
• Version Model Number: 10440
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does n
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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	00616784044018 [Primary]

FDA Product Code

• FNM: Mattress, Air Flotation, Alternating Pressure

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: 2018-06-20
• Device Publish Date: 2018-05-20

On-Brand Devices [Air Mattress, Dial Operated Pump, w/Bubble Pad]

• 00616784044019: 10440
• 00616784044018: 10440