Verathon

GUDID 00810041638434

Provision

Rigid intubation laryngoscope, single-use

• Primary Device ID: 00810041638434
• NIH Device Record Key: 6f3357d2-fe7d-4c71-b307-df8d55783e6c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Verathon
• Version Model Number: 0574-0026
• Company DUNS: 016889401
• Company Name: Provision
• Device Count: 1
• DM Exempt: true
• 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: true
• 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	00810041638434 [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: 2020-08-11
• Device Publish Date: 2020-08-03

On-Brand Devices [Verathon]

• B504LG057401100: 0574-0110
• B504LG057401040: 0574-0104
• B504LG057401010: 0574-0101
• B504LG057401000: 0574-0100
• B504LG057400270: 0574-0027
• B504LG057400260: 0574-0026
• 00810041638472: 0574-0101
• 00810041638465: 0574-0100
• 00810041638458: 0574-0110
• 00810041638441: 0574-0027
• 00810041638434: 0574-0026
• 00810041638427: 0574-0104
• B504GS080006080: 0800-0608
• B504GS027006810: 0270-0681
• B504GS080300090: 0803-0009
• B504LG057401950: 0574-0195
• B504LG057401660: 0574-0166
• B504LG057401650: 0574-0165
• B504GS080301180: 0803-0118