DIY

GUDID B347DIYFLEX1

LED TECHNOLOGIES INC

Blue/red/infrared phototherapy lamp

• Primary Device ID: B347DIYFLEX1
• NIH Device Record Key: d0f96c1c-7ec6-4b66-90da-2c014727ae31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DIY
• Version Model Number: DIYFLEX
• Company DUNS: 197386191
• Company Name: LED TECHNOLOGIES INC
• 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: 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	B347DIYFLEX0 [Primary]
HIBCC	B347DIYFLEX1 [Package]; Contains: B347DIYFLEX0; Package: [20 Units]; In Commercial Distribution

FDA Product Code

• ILY: Lamp, Infrared, Therapeutic Heating

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-10-03

On-Brand Devices [DIY]

• B347DIYMITT1: DIYMITT
• B347DIYFLEX1: DIYFLEX