Flex Extenders

GUDID 10709078008280

Flex Extenders 5.2" x 15mm x 22mm x 15mm

WESTMED, INC.

Anaesthesia breathing circuit, single-use

• Primary Device ID: 10709078008280
• NIH Device Record Key: 25cd99e1-8253-45fc-8bc3-a990765398d5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Flex Extenders
• Version Model Number: S6419P
• Company DUNS: 092673953
• Company Name: WESTMED, 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: 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	00709078008283 [Primary]
GS1	10709078008280 [Package]; Contains: 00709078008283; Package: [50 Units]; In Commercial Distribution

FDA Product Code

• CAI: Circuit, Breathing (W Connector, Adaptor, Y Piece)

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: 2020-03-09
• Device Publish Date: 2020-02-28

On-Brand Devices [Flex Extenders]

• 00709078004643: 2179
• 10709078008280: Flex Extenders 5.2" x 15mm x 22mm x 15mm
• 10709078008402: Flex Extender, 5.2" x 15mm OD x 22/15mm ID