BriteBlade Pro

GUDID 05055788771647

BriteBlade Pro Single-Use Fiber Optic Curved Miller 2

FLEXICARE MEDICAL LIMITED

Laryngoscope blade, single-use

• Primary Device ID: 05055788771647
• NIH Device Record Key: 7abf3d3b-9241-4f3b-99dd-94ecb46bbfd0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BriteBlade Pro
• Version Model Number: 040-00-0421U
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05055788771647 [Primary]

FDA Product Code

• CCW: Laryngoscope, Rigid

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-03-25
• Device Publish Date: 2024-03-15

On-Brand Devices [BriteBlade Pro]

• 05055931101000: BriteBlade Pro Single Use Fiber Optic Centerline Miller Blade Size 4
• 05055931100980: BriteBlade Pro Single Use Fiber Optic Centerline Miller Blade Size 3
• 05055931100225: BriteBlade Pro Single Use Fiber Optic Centerline Miller 2
• 05055788771647: BriteBlade Pro Single-Use Fiber Optic Curved Miller 2