Dr. Don's Upper Arm Suspension

GUDID 10840113230706

Intended to support and maintain the position of an anesthetized patient during surgery

ASPEN SURGICAL PRODUCTS, INC.

Arm procedure positioner, single-use Arm procedure positioner, single-use Arm procedure positioner, single-use Arm procedure positioner, single-use Arm procedure positioner, single-use Arm procedure positioner, single-use Arm procedure positioner, single-use Arm procedure positioner, single-use Arm procedure positioner, single-use Arm procedure positioner, single-use Arm procedure positioner, single-use Arm procedure positioner, single-use Arm procedure positioner, single-use Arm procedure positioner, single-use Arm procedure positioner, single-use Arm procedure positioner, single-use

• Primary Device ID: 10840113230706
• NIH Device Record Key: 44520e51-d432-4694-8617-55a60a97cad4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dr. Don's Upper Arm Suspension
• Version Model Number: 711502
• Company DUNS: 027680821
• Company Name: ASPEN SURGICAL 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: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• 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: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840113230709 [Primary]
GS1	10840113230706 [Package]; Contains: 00840113230709; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• CCX: SUPPORT, PATIENT POSITION

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-03-30
• Device Publish Date: 2021-03-22