Exer Physio

GUDID G186EXERPHYSIO20

Exer Labs, Inc.

Self-care monitoring/reporting software

• Primary Device ID: G186EXERPHYSIO20
• NIH Device Record Key: 7d45e1b4-0254-447a-96ec-b47b0d8ecb59
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Exer Physio
• Version Model Number: 2
• Company DUNS: 069864301
• Company Name: Exer Labs, Inc.
• 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: false
• 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
HIBCC	G186EXERPHYSIO20 [Primary]

FDA Product Code

• QKC: Interactive Rehabilitation Exercise Device, Prescription Use

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: 2022-01-12
• Device Publish Date: 2022-01-04

Devices Manufactured by Exer Labs, Inc.

• G186EXERSCAN20 - Exer Scan: 2024-09-11
• G186EXERHEALTH20 - Exer Health: 2023-03-29
• G186EXERGAIT10 - Exer Gait: 2022-05-30
• G186EXERPHYSIO20 - Exer Physio: 2022-01-12
• G186EXERPHYSIO20 - Exer Physio: 2022-01-12