DynaTrack Plus-CLFLEX

GUDID 00802357170272

MEDICAL SPECIALTIES INCORPORATED

Knee support orthosis

• Primary Device ID: 00802357170272
• NIH Device Record Key: b53d0cdf-f218-45ce-ab1b-519266462808
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DynaTrack Plus-CLFLEX
• Version Model Number: 117027
• Company DUNS: 003173028
• Company Name: MEDICAL SPECIALTIES INCORPORATED
• 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: true
• Serial Number: false
• Manufacturing Date: true
• 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	00802357170272 [Primary]

FDA Product Code

• ITQ: Joint, Knee, External Brace

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: 2022-12-15
• Device Publish Date: 2022-12-07

On-Brand Devices [DynaTrack Plus-CLFLEX]

• 00802357170289: 117028
• 00802357170272: 117027
• 00802357170265: 117026
• 00802357170258: 117025
• 00802357170241: 117024
• 00802357170227: 117022
• 00802357170210: 117021