Berman Airways (color coded)

GUDID 30641043800502

MERCURY ENTERPRISES, INC.

Oropharyngeal airway, single-use

• Primary Device ID: 30641043800502
• NIH Device Record Key: 2287a98a-c2c5-40f6-ae95-c46dfe36cdb0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Berman Airways (color coded)
• Version Model Number: 10-800-50C
• Company DUNS: 032705659
• Company Name: MERCURY ENTERPRISES, INC.
• 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: true
• 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	10641043800508 [Primary]
GS1	30641043800502 [Package]; Contains: 10641043800508; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• CAE: Airway, Oropharyngeal, Anesthesiology

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: 2020-08-07
• Device Publish Date: 2020-07-30

On-Brand Devices [Berman Airways (color coded)]

• 30641043800908: 10-800-90C
• 30641043800809: 10-800-80C
• 30641043800700: 10-800-70C
• 30641043800601: 10-800-60C
• 30641043800502: 10-800-50C
• 30641043800403: 10-800-40C
• 30641043800106: 10-800-10C
• 30641043800007: 10-800-00C
• 30641043815902: 90MM
• 30641043815803: 80MM
• 30641043815704: 70MM
• 30641043815605: 60MM
• 30641043815506: 50MM
• 30641043815407: 40MM
• 30641043815100: 110MM
• 30641043815001: 100MM