Alexis® Orthopaedic Protector

GUDID 10607915138957

S/M Flexible Alexis Orthopaedic Protector

APPLIED MEDICAL RESOURCES CORPORATION

Radial surgical retractor

• Primary Device ID: 10607915138957
• NIH Device Record Key: fa2f8950-7506-43a8-b73c-cf2172cddddc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Alexis® Orthopaedic Protector
• Version Model Number: HR104
• Company DUNS: 187129135
• Company Name: APPLIED MEDICAL RESOURCES 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 19497138300
• Email: contact@appliedmedical.com
• Phone: 19497138300
• Email: contact@appliedmedical.com
• Phone: 19497138300
• Email: contact@appliedmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00607915138950 [Primary]
GS1	10607915138957 [Package]; Contains: 00607915138950; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• KGW: Ring (Wound Protector), Drape Retention, Internal

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: 2018-09-13
• Device Publish Date: 2018-08-13

On-Brand Devices [Alexis® Orthopaedic Protector]

• 10607915138964: M/L Flexible Alexis Orthopaedic Protector
• 10607915138957: S/M Flexible Alexis Orthopaedic Protector
• 10607915138940: S/S Flexible Alexis Orthopaedic Protector