Sacroiliac Belt

GUDID 00802357000159

MEDICAL SPECIALTIES INCORPORATED

Lumbar spine orthosis

• Primary Device ID: 00802357000159
• NIH Device Record Key: cc04f1e8-a029-4b1c-9b32-8b283e0dc152
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sacroiliac Belt
• Version Model Number: 163307-I
• 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	00802357000159 [Primary]

FDA Product Code

• IPY: Orthosis, Lumbo-Sacral

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: 2023-07-13
• Device Publish Date: 2023-07-05

On-Brand Devices [Sacroiliac Belt]

• 00802357000111: 163302-I
• 00080235700159: 163307-I
• 00080235700142: 163306-I
• 00080235700135: 163305-I
• 00080235700128: 163304-I
• 00802357000159: 163307-I
• 00802357000142: 163306-I
• 00802357000135: 163305-I
• 00802357000128: 163304-I