DALTON WALKER

GUDID 00815027012796

WALKER HEMI

DALTON MEDICAL CORPORATION

Handgrip disability-assistive walker, non-powered, foldable

• Primary Device ID: 00815027012796
• NIH Device Record Key: b179adc6-2e63-481c-a5c4-6d460e828778
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DALTON WALKER
• Version Model Number: A-WA6005HEM
• Company DUNS: 874709348
• Company Name: DALTON MEDICAL 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: true
• 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	00815027012796 [Primary]

FDA Product Code

• ITJ: Walker, Mechanical

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: 2025-09-26
• Device Publish Date: 2025-09-18

On-Brand Devices [DALTON WALKER ]

• 00815027012796: WALKER HEMI
• 00815027012789: WALKER WITH WHEEL, FOLDING