10476 - Headboard/Footboard, Long Term Care beds, Amber Cherry, 1pr/Cs

GUDID 00616784047638

DYNAREX CORPORATION

Electrical assistive bed

• Primary Device ID: 00616784047638
• NIH Device Record Key: aae54526-f8f0-43f1-978d-43ffa7ad3eac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 10476 - Headboard/Footboard, Long Term Care beds, Amber Cherry, 1pr/Cs
• Version Model Number: 10476
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00616784047638 [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: 2018-10-11
• Device Publish Date: 2018-09-10

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• 00616784191119 - DynaFit Graduated Compression Anti-Embolism Stocking, Medium Knee: 2025-10-06
• 00616784191218 - DynaFit Graduated Compression Anti-Embolism Stocking, Large Knee: 2025-10-06
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