ELASTIC ANKLE SUPPORT XL

GUDID 00840314811196

Hausmann Enterprises, LLC

Ankle/foot orthosis

• Primary Device ID: 00840314811196
• NIH Device Record Key: 99ea864c-f639-423f-9624-8133d7496248
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ELASTIC ANKLE SUPPORT XL
• Version Model Number: HM0133
• Company DUNS: 001892660
• Company Name: Hausmann Enterprises, LLC
• 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: 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	00840314811196 [Primary]

FDA Product Code

• ITW: Joint, Ankle, 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: 2025-01-09
• Device Publish Date: 2025-01-01

Devices Manufactured by Hausmann Enterprises, LLC

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• 00840314812308 - F8X LACER ANKLE W/STAYS LG: 2025-01-10
• 00840314811097 - UNIV ARM SLING W/FOAM STRAP ADULT: 2025-01-09
• 00840314811165 - ELASTIC ANKLE SUPPORT SM: 2025-01-09
• 00840314811172 - ELASTIC ANKLE SUPPORT MD: 2025-01-09
• 00840314811189 - ELASTIC ANKLE SUPPORT LG: 2025-01-09
• 00840314811196 - ELASTIC ANKLE SUPPORT XL: 2025-01-09
• 00840314811196 - ELASTIC ANKLE SUPPORT XL: 2025-01-09
• 00840314811202 - ELASTIC ELBOW SUPPORT SM: 2025-01-09