INFRABALDAN

GUDID 08053782383313

B&M SRL MARKETING NEL BENESSERE

Red/infrared light phototherapy unit

• Primary Device ID: 08053782383313
• NIH Device Record Key: eae6bd84-cdff-4364-99c3-3b023ba0f661
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INFRABALDAN
• Version Model Number: INFRABALDAN
• Company DUNS: 445139129
• Company Name: B&M SRL MARKETING NEL BENESSERE
• 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: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08053782383313 [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: 2025-05-08
• Device Publish Date: 2025-04-30

Devices Manufactured by B&M SRL MARKETING NEL BENESSERE

• 08053782383313 - INFRABALDAN: 2025-05-08
• 08053782383313 - INFRABALDAN: 2025-05-08
• 08053782383283 - T-SHAPE 2: 2025-04-21