AMERILUX

GUDID M368ALX421

Low Height Bed 42"

GF HEALTH PRODUCTS, INC.

Basic electric hospital bed

• Primary Device ID: M368ALX421
• NIH Device Record Key: 8f475788-6434-4b0d-8567-9f0e72aeca61
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AMERILUX
• Version Model Number: ALX42
• Company DUNS: 132016168
• Company Name: GF HEALTH PRODUCTS, INC.
• 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: true
• 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

Customer Support Contacts

• Phone: 770-368-4700
• Email: CS@grahamfield.com
• Phone: 770-368-4700
• Email: CS@grahamfield.com
• Phone: 770-368-4700
• Email: CS@grahamfield.com
• Phone: 770-368-4700
• Email: CS@grahamfield.com
• Phone: 770-368-4700
• Email: CS@grahamfield.com
• Phone: 770-368-4700
• Email: CS@grahamfield.com
• Phone: 770-368-4700
• Email: CS@grahamfield.com
• Phone: 770-368-4700
• Email: CS@grahamfield.com
• Phone: 770-368-4700
• Email: CS@grahamfield.com
• Phone: 770-368-4700
• Email: CS@grahamfield.com
• Phone: 770-368-4700
• Email: CS@grahamfield.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M368ALX421 [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: 2025-12-19
• Device Publish Date: 2025-12-11

On-Brand Devices [AMERILUX]

• M368ALX421: Low Height Bed 42"
• M368ALX361: Low Height Bed 36"