BriteBlade Pro Evo Single-Use Fiber Optic Miller 1

GUDID 15055788722523

FLEXICARE MEDICAL LIMITED

Laryngoscope blade, single-use

• Primary Device ID: 15055788722523
• NIH Device Record Key: 8d1f8794-1b07-440e-9fd1-8ab091f17329
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BriteBlade Pro Evo Single-Use Fiber Optic Miller 1
• Version Model Number: 040-761U
• Company DUNS: 504406273
• Company Name: FLEXICARE MEDICAL LIMITED
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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
GS1	15055788722523 [Primary]

FDA Product Code

• CCW: Laryngoscope, Rigid

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: 2024-08-15
• Device Publish Date: 2024-08-07

On-Brand Devices [BriteBlade Pro Evo Single-Use Fiber Optic Miller 1]

• 05055788722526: 040-761U
• 15055788722523: 040-761U