UNIVERSAL FLEX2®BREATHING CIRCUIT & PACK KIT F94488

GUDID 00612649176796

UNIVERSAL FLEX2 PACK KIT

King Systems Corporation

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• Primary Device ID: 00612649176796
• NIH Device Record Key: 155f371c-0437-43e2-a02c-ac60ad1136eb
• Commercial Distribution Discontinuation: 2019-10-10
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: UNIVERSAL FLEX2®BREATHING CIRCUIT & PACK KIT
• Version Model Number: F94488
• Catalog Number: F94488
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00612649176796 [Package]; Contains: 00612649203294; Package: [40 Units]; Discontinued: 2019-10-10; Not in Commercial Distribution
GS1	00612649203294 [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: 5
• Public Version Date: 2019-11-27
• Device Publish Date: 2016-09-22

On-Brand Devices [UNIVERSAL FLEX2®BREATHING CIRCUIT & PACK KIT]

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• 00612649208749: UNIVERSAL FLEX2 PACK KIT 40/CS
• 00612649184425: UNIVERSAL FLEX2 CIRCUIT & PACK KIT 40/CS
• 00612649183176: UNIVERSAL FLEX2 PACK KIT 50/CS
• 00612649183145: UNIVERSAL FLEX2 PACK KIT 15/CS
• 00612649181431: UNIVERSAL FLEX2 PACK KIT 50/CS
• 00612649181172: UNIVERSAL FLEX2 PACK KIT
• 00612649180847: UNIVERSAL FLEX2 PACK KIT
• 00612649180861: UNIVERSAL FLEX2 PACK KIT
• 00612649183886: UNIVERSAL FLEX2 PACK KIT 40/CS
• 00612649179957: UNIVERSAL FLEX2 PACK KIT
• 00612649180496: UNIVERSAL FLEX2 PACK KIT
• 00612649178004: UNIVERSAL FLEX2 PACK KIT
• 00612649176871: UNIVERSAL FLEX2 PACK KIT
• 00612649176796: UNIVERSAL FLEX2 PACK KIT
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• 00612649171807: UNIVERSAL FLEX2 PACK KIT
• 00612649171258: UNIVERSAL FLEX2 CIRCUIT
• 00612649170626: UNIVERSAL FLEX2 PACK KIT
• 00612649171500: UNIVERSAL FLEX2 PACK KIT
• 00612649170053: UNIVERSAL FLEX2 PACK KIT
• 00612649169002: UNIVERSAL FLEX2 PACK KIT
• 00612649168920: UNIVERSAL FLEX2 PACK KIT
• 00612649168739: UNIVERSAL FLEX2 PACK KIT
• 00612649168746: UNIVERSAL FLEX2 PACK KIT
• 00612649168197: UNIVERSAL FLEX2 PACK KIT
• 00612649166964: UNIVERSAL FLEX2 PACK KIT
• 00612649166339: UNIVERSAL FLEX2 PACK KIT
• 00612649165592: UNIVERSAL FLEX2 PACK KIT
• 00612649165332: UNIVERSAL FLEX2 PACK KIT
• 00612649162133: UNIVERSAL FLEX2 CIRCUIT