bili-hut™ global

GUDID 00850019925241

LITTLE SPARROWS TECHNOLOGIES LLC

Overhead infant phototherapy unit

• Primary Device ID: 00850019925241
• NIH Device Record Key: 18ce5f3e-7244-4869-b492-67e9a5994076
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: bili-hut™ global
• Version Model Number: 0130AG
• Company DUNS: 078764736
• Company Name: LITTLE SPARROWS TECHNOLOGIES LLC
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850019925241 [Primary]

FDA Product Code

• LBI: Unit, Neonatal Phototherapy

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: 2021-02-08
• Device Publish Date: 2021-01-29

On-Brand Devices [bili-hut™ global]

• 00850019925258: 0130AG
• 00850019925241: 0130AG
• 00850019925234: 0130AG
• 00850019925227: 0130AG
• 00850019925210: 0130AG
• 00850019925203: 0130AG