Flex Extenders

GUDID 00709078004643

WESTMED, INC.

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• Primary Device ID: 00709078004643
• NIH Device Record Key: f6745ad4-f366-40f7-b5c2-926c4850100a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Flex Extenders
• Version Model Number: 2179
• Company DUNS: 092673953
• Company Name: WESTMED, INC.
• Device Count: 200
• 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	00709078004643 [Primary]
GS1	00709078004650 [Unit of Use]

FDA Product Code

• BZA: Connector, Airway (Extension)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-01-23
• Device Publish Date: 2017-12-27

On-Brand Devices [Flex Extenders]

• 00709078004643: 2179
• 10709078008280: Flex Extenders 5.2" x 15mm x 22mm x 15mm