SpectraLite

GUDID B347BA5670102

LED TECHNOLOGIES INC

Blue/red/infrared phototherapy lamp

• Primary Device ID: B347BA5670102
• NIH Device Record Key: 7b5ac0b6-f47b-4d68-83cb-b4f37a2556b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SpectraLite
• Version Model Number: BA567010
• 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	B347BA5670100 [Primary]
HIBCC	B347BA5670101 [Package]; Contains: B347BA5670100; Package: [3 Units]; In Commercial Distribution
HIBCC	B347BA5670102 [Package]; Contains: B347BA5670101; Package: [8 Units]; In Commercial Distribution

FDA Product Code

• OHS: Light Based Over The Counter Wrinkle Reduction

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: 2017-01-23

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