BELA MD+ AQUA TIP

GUDID 00754016214103

Luvo Medical Technologies Inc

Analgesic transcutaneous electrical nerve stimulation system

• Primary Device ID: 00754016214103
• NIH Device Record Key: 1d0405ad-fdf2-425e-8ae9-3382a2059af0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BELA MD+ AQUA TIP
• Version Model Number: ES2587
• Company DUNS: 204046564
• Company Name: Luvo Medical Technologies 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: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00754016214103 [Primary]

FDA Product Code

• GFE: Brush, Dermabrasion, Powered

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: 2021-06-09
• Device Publish Date: 2021-06-01

On-Brand Devices [BELA MD+ AQUA TIP]

• 00754016214103: ES2587
• 00754016214097: ES2586