Shoulder Traction Kit; PL

GUDID 20787551000485

XODUS MEDICAL, INC.

Upper-limb traction wrap/trap, single-use, sterile

• Primary Device ID: 20787551000485
• NIH Device Record Key: 64901c38-1c9f-46c2-b1c3-85ea66b9da6d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Shoulder Traction Kit; PL
• Version Model Number: 90403BIO
• Company DUNS: 868042664
• Company Name: XODUS MEDICAL, INC.
• Device Count: 6
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• 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

Customer Support Contacts

• Phone: +1(724)337-5500
• Email: info@xodusmedical.com
• Phone: +1(724)337-5500
• Email: info@xodusmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00787551000481 [Unit of Use]
GS1	20787551000485 [Primary]

FDA Product Code

• KQZ: COMPONENT, TRACTION, NON-INVASIVE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-05-02

On-Brand Devices [Shoulder Traction Kit; PL]

• 20787551000485: 90403BIO
• 00787551000481: Shoulder Traction Kit; PL