UNIVERSAL F® FLEXBREATHING CIRCUIT KNUF375-6121Z21

GUDID 00612649184227

UNIVERSAL F FLEX CIRCUT 50/CS

King Systems Corporation

Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use Anaesthesia breathing circuit, single-use

• Primary Device ID: 00612649184227
• NIH Device Record Key: dbedbee2-f934-4e9b-9def-20dc3e4e921e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UNIVERSAL F® FLEXBREATHING CIRCUIT
• Version Model Number: KNUF375-6121Z21
• Catalog Number: KNUF375-6121Z21
• 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: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com
• Phone: +13177763175
• Email: wnet@ambu.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00612649184227 [Package]; Contains: 00612649204963; Package: [50 Units]; In Commercial Distribution
GS1	00612649204963 [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: 3
• Public Version Date: 2019-11-27
• Device Publish Date: 2016-09-22

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