King Vision Video Laryngoscope Standard aBlade KVLAB3

GUDID 00612649182094

King Vision - aBlades size 3 20 pcs. = 1 case

King Systems Corporation

Rigid optical laryngopharyngoscope

• Primary Device ID: 00612649182094
• NIH Device Record Key: 54189e37-5991-4da0-8a6e-21f3b8a179a1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: King Vision Video Laryngoscope Standard aBlade
• Version Model Number: KVLAB3
• Catalog Number: KVLAB3
• Company DUNS: 009299017
• Company Name: King Systems Corporation
• Device Count: 20
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• 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	00612649181226 [Primary]
GS1	00612649182094 [Package]; Contains: 00612649181226; Package: [3 Units]; In Commercial Distribution
GS1	00612649182162 [Unit of Use]

FDA Product Code

• CCW: LARYNGOSCOPE, RIGID

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: 2023-11-17
• Device Publish Date: 2022-12-08

Devices Manufactured by King Systems Corporation

• 00612649216942 - UNIVERSAL FLEX2®: 2024-12-09 UNIVERSAL FLEX2 CIRCUIT
• 00612649216966 - UNIVERSAL FLEX2®BREATHING CIRCUIT: 2024-12-09 UNIVERSAL FLEX2 CIRCUIT
• 00612649216980 - UNIVERSAL FLEX2®BREATHING CIRCUIT: 2024-12-09 UNIVERSAL FLEX2 CIRCUIT
• 00612649217000 - UNIVERSAL FLEX2®: 2024-12-09 UNIVERSAL FLEX2 CIRCUIT
• 00612649217024 - UNIVERSAL FLEX2®: 2024-12-09 UNIVERSAL FLEX2 CIRCUIT
• 00612649217048 - UNIVERSAL FLEX2®: 2024-12-09 UNIVERSAL FLEX2 CIRCUIT
• 00612649217062 - UNIVERSAL FLEX2®: 2024-12-09 UNIVERSAL FLEX2 CIRCUIT
• 00612649217086 - UNIVERSAL FLEX2®: 2024-12-09 UNIVERSAL FLEX2 CIRCUIT