Berman Oral Airway

GUDID 10709078014052

Standard Berman Oral Airway 50mm (Individually Bagged)

WESTMED, INC.

Oesophageal-obturating/tracheal airway, single-use

• Primary Device ID: 10709078014052
• NIH Device Record Key: a1c94533-71d2-4581-90b3-19e31e2378cf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Berman Oral Airway
• Version Model Number: 1002263
• Company DUNS: 092673953
• Company Name: WESTMED, INC.
• Device Count: 50
• 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00709078014048 [Primary]
GS1	10709078014052 [Unit of Use]

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: 2022-04-08
• Device Publish Date: 2022-03-31

On-Brand Devices [Berman Oral Airway]

• 00709078007002: Berman Oral Airway, 100mm, Individually Bagged
• 00709078006982: Berman Oral Airway 90 mm
• 00709078006968: Berman Oral Airway, 80 mm, Individually Bagged
• 00709078006920: Standard Berman Oral Airway, 60 mm, Individually Bagged
• 00709078006906: Standard Berman Oral Airway, 50 mm, Individually Bagged
• 00709078006883: Standard Oral Berman Oral Airway 40 mm
• 10709078014489: Standard Berman Oral Airway 100mm (Individually Bagged) (TwinMed)
• 10709078014465: Standard Berman Oral Airway 80mm (Individually Bagged) (TwinMed)
• 10709078014052: Standard Berman Oral Airway 50mm (Individually Bagged)