XL Cone

GUDID 00854103007240

BDA Attachment XL Cone

LITECURE LLC

Musculoskeletal/physical therapy laser beam guide tip, transcutaneous

• Primary Device ID: 00854103007240
• NIH Device Record Key: 372a282a-50c5-4b38-8911-dc01f5ac0608
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: XL Cone
• Version Model Number: PRD-000644-000-L
• Company DUNS: 858768943
• Company Name: LITECURE LLC
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00854103007240 [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: 2022-07-08
• Device Publish Date: 2022-06-30

On-Brand Devices [XL Cone]

• 00854103007240: BDA Attachment XL Cone
• 00854103007318: BDA Attachment XL Cone