ProVu Video Stylet 038-995-080U

GUDID 05055788776307

ProVu Video Stylet with Reinforced ET Tube Size 8.0

FLEXICARE MEDICAL LIMITED

Video-intubation endotracheal tube

• Primary Device ID: 05055788776307
• NIH Device Record Key: 4d4bdd3e-f82e-465c-a89b-98790550777e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProVu Video Stylet
• Version Model Number: 038-995-080U
• Catalog Number: 038-995-080U
• Company DUNS: 504406273
• Company Name: FLEXICARE MEDICAL LIMITED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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	05055788776307 [Primary]

FDA Product Code

• BTR: Tube, Tracheal (W/Wo Connector)

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: 2025-06-09
• Device Publish Date: 2025-05-30

On-Brand Devices [ProVu Video Stylet]

• 05055788776307: ProVu Video Stylet with Reinforced ET Tube Size 8.0
• 05055788776284: ProVu Video Stylet with Reinforced ET Tube Size 7.5
• 05055788776260: ProVu Video Stylet with Reinforced ET Tube Size 7.0
• 05055788776246: ProVu Video Stylet with Reinforced ET Tube Size 6.5