DALTON WIDE MANUAL WHEELCHAIR

GUDID 00815027010846

WHEELCHAIR, MANUAL, 22" W/FOOTREST, HEAVY DUTY, WT LIMIT 350 LBS

DALTON MEDICAL CORPORATION

Wheelchair, occupant-driven, rear-wheels-operated, collapsible

• Primary Device ID: 00815027010846
• NIH Device Record Key: 31e13efb-19e1-446d-be4e-34ecbed6efda
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DALTON WIDE MANUAL WHEELCHAIR
• Version Model Number: K07DK22F02V
• Company DUNS: 874709348
• Company Name: DALTON MEDICAL CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	00815027010846 [Primary]

FDA Product Code

• IOR: Wheelchair, 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: 2020-05-06
• Device Publish Date: 2020-04-28

On-Brand Devices [DALTON WIDE MANUAL WHEELCHAIR]

• 00815027010877: WHEELCHAIR, MANUAL, 24" W/LEGREST, HEAVY DUTY, WT LIMIT 400 LBS
• 00815027010860: WHEELCHAIR, MANUAL, 24" W/FOOTREST, HEAVY DUTY, WT LIMIT 400 LBS
• 00815027010853: WHEELCHAIR, MANUAL, 22" W/LEGREST, HEAVY DUTY, WT LIMIT 350 LBS
• 00815027010846: WHEELCHAIR, MANUAL, 22" W/FOOTREST, HEAVY DUTY, WT LIMIT 350 LBS
• 00815027010839: WHEELCHAIR, MANUAL, W/LEGREST, WT LIMIT 310 LBS
• 00815027010822: WHEELCHAIR,MANUAL, 20" W/FOOTREST, WT LIMIT 310LBS