TRIPOD WRIST LACER II

GUDID 00802357240012

MEDICAL SPECIALTIES INCORPORATED

Wrist orthosis

• Primary Device ID: 00802357240012
• NIH Device Record Key: 36f5a3f3-324d-45ed-9927-dd9f097b5ca5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TRIPOD WRIST LACER II
• Version Model Number: 224001
• 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	00802357240012 [Primary]

FDA Product Code

• ILH: Splint, Hand, And Components

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: 2025-01-22
• Device Publish Date: 2025-01-14

On-Brand Devices [TRIPOD WRIST LACER II]

• 00802357240166: 224016
• 00802357240159: 224015
• 00802357240142: 224014
• 00802357240128: 224012
• 00802357240111: 224011
• 00802357240067: 224006
• 00802357240050: 224005
• 00802357240043: 224004
• 00802357240029: 224002
• 00802357240012: 224001