Berman Oral Airway

GUDID 00709078006982

Berman Oral Airway 90 mm

WESTMED, INC.

Oesophageal-obturating/tracheal airway, single-use

• Primary Device ID: 00709078006982
• NIH Device Record Key: 76cd9cec-b493-4158-a8ef-874dd289c39b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Berman Oral Airway
• Version Model Number: 7-2091
• 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: true
• Serial Number: false
• 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	00709078006982 [Primary]
GS1	10709078006989 [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: 2019-05-14
• Device Publish Date: 2019-05-06

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)