UNIVERSAL F® FLEXBREATHING CIRCUIT FF376-6121Z

GUDID 00612649213545

UNIVERSAL F FLEX CIRCUIT

King Systems Corporation

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• Primary Device ID: 00612649213545
• NIH Device Record Key: f338fec2-ca65-4850-a117-6f6ee0b42d41
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UNIVERSAL F® FLEXBREATHING CIRCUIT
• Version Model Number: FF376-6121Z
• Catalog Number: FF376-6121Z
• Company DUNS: 009299017
• Company Name: King Systems Corporation
• 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: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com
• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00612649213545 [Package]; Contains: 00612649213552; Package: [50 Units]; In Commercial Distribution
GS1	00612649213552 [Primary]

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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-11-27
• Device Publish Date: 2019-01-29

On-Brand Devices [UNIVERSAL F® FLEXBREATHING CIRCUIT]

• 00612649213545: UNIVERSAL F FLEX CIRCUIT
• 00612649213118: Universal F Flex Breathing Circuit
• 00612649213071: Universal F Flex Breathing Circuit
• 00612649213064: Universal F Flex Breathing Circuit
• 00612649209944: UNIVERSAL F FLEX CIRCUIT
• 00612649184296: UNIVERSAL F FLEX CIRCUT 50/CS
• 00612649180991: UNIVERSAL F FLEX CIRCUIT
• 00612649184227: UNIVERSAL F FLEX CIRCUT 50/CS
• 00612649179018: UNIVERSAL F FLEX CIRCUIT
• 00612649179568: UNIVERSAL F FLEX CIRCUIT
• 00612649179827: UNIVERSAL F FLEX CIRCUIT 50/CS