Sacroiliac Belt

GUDID 00080235700135

MEDICAL SPECIALTIES INCORPORATED

Lumbar spine orthosis

• Primary Device ID: 00080235700135
• NIH Device Record Key: b3b5dc54-2c96-4f75-8771-63e24018cc98
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sacroiliac Belt
• Version Model Number: 163305-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	00080235700135 [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: 2022-12-15
• Device Publish Date: 2022-12-07

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