LIGHTFORCE

GUDID 00190446887195

R-800um SHP v2 Assy Light Force

DJO, LLC

Musculoskeletal/physical therapy laser beam guide, transcutaneous

• Primary Device ID: 00190446887195
• NIH Device Record Key: a7e86c85-6b85-4a90-9a80-110e61aec213
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIGHTFORCE
• Version Model Number: PRD-000758-010-00-L-R
• Company DUNS: 081840873
• Company Name: DJO, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00190446887195 [Primary]

FDA Product Code

• ILY: Lamp, infrared, therapeutic heating

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: 2024-09-23
• Device Publish Date: 2024-09-13

On-Brand Devices [LIGHTFORCE]

• 00190446887195: R-800um SHP v2 Assy Light Force
• 00190446897910: Trade-In 800um SHP v2 Assy LightForce - less than 5 yrs old
• 00190446897903: Trade-In 800um SHP v2 Assy LightForce - more than 5 yrs old
• 00190446897859: Trade-In 600um BHP LightForce - less than 5yrs old
• 00190446897842: Trade-In 600um BHP LightForce - More than 5yrs old
• 00190446812142: LightForce X 10W