David Scott Company

GUDID 15060797554249

Robotic Stirrups

David Scott Company

Heel stirrup Heel stirrup Heel stirrup Heel stirrup Heel stirrup Heel stirrup Heel stirrup Heel stirrup Heel stirrup Heel stirrup Heel stirrup Heel stirrup Heel stirrup Heel stirrup Heel stirrup Heel stirrup Heel stirrup

• Primary Device ID: 15060797554249
• NIH Device Record Key: 6c8ac900-d5b0-4bf9-8e4d-1bc8be27c402
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: David Scott Company
• Version Model Number: DSC-800-0342-R
• Company DUNS: 073814568
• Company Name: David Scott Company
• 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: false
• 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	15060797554249 [Primary]

FDA Product Code

• CCX: Support, Patient Position

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: 2024-02-26
• Device Publish Date: 2024-02-16

On-Brand Devices [David Scott Company]

• 15060797554102: Arthroscopic Leg Holder
• 15060797554089: Shoulder Support
• 15060797554010: Picket Fence Leg Holder
• 15060797554003: Double Post Picket Fence Leg Holder
• 15060797554249: Robotic Stirrups
• 15060797554188: Carbon Fiber Anesthesia Armboard