Universal Q-Bar Bed Rail

GUDID 00616784046525

DYNAREX CORPORATION

Bedrail

• Primary Device ID: 00616784046525
• NIH Device Record Key: 031c5b66-7aa7-4497-875a-00206b6959e6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Universal Q-Bar Bed Rail
• Version Model Number: 10465
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• Device Count: 2
• 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: 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	00616784046518 [Unit of Use]
GS1	00616784046525 [Primary]

FDA Product Code

• FNL: Bed, Ac-Powered Adjustable Hospital

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: 2018-06-19
• Device Publish Date: 2018-05-19

Devices Manufactured by DYNAREX CORPORATION

• 00810180840163 - DynaSafety Cotton-Tipped Applicators in Sealed Vial,3": 2024-11-19
• 00840117341210 - Medicine Cups 1oz: 2024-11-05
• 00840117312906 - Resp-O2 Endotracheal Tube Cuffed, 4.0 mm: 2024-11-01 Sterile-EO
• 00840117312920 - Resp-O2 Endotracheal Tube Cuffed, 4.5 mm: 2024-11-01 Sterile-EO
• 00840117317475 - Resp-O2 Endotracheal Tube Cuffed, 5.0 mm: 2024-11-01 Sterile-EO
• 00840117312968 - Resp-O2 Endotracheal Tube Cuffed, 5.5 mm: 2024-11-01 Sterile-Eo
• 00840117312982 - Resp-O2 Endotracheal Tube Cuffed, 6.0 mm: 2024-11-01 Sterile-Eo
• 00840117313002 - Resp-O2 Endotracheal Tube Cuffed, 6.5 mm: 2024-11-01 Sterile-Eo