ADULT ULTRA FLEX® 6752BF-13221

GUDID 00612649214870

ADULT ULTRAFLEX CIRCUIT

King Systems Corporation

Anaesthesia breathing circuit, single-use

• Primary Device ID: 00612649214870
• NIH Device Record Key: 48a1a7fb-e811-491f-ba85-3fbfefbdddbe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ADULT ULTRA FLEX®
• Version Model Number: 6752BF-13221
• Catalog Number: 6752BF-13221
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(410)768-6464
• Email: Purchase_orders@ambuUSA.com
• Phone: +1(410)768-6464
• Email: Purchase_orders@ambuUSA.com
• Phone: +1(410)768-6464
• Email: Purchase_orders@ambuUSA.com
• Phone: +1(410)768-6464
• Email: Purchase_orders@ambuUSA.com
• Phone: +1(410)768-6464
• Email: Purchase_orders@ambuUSA.com
• Phone: +1(410)768-6464
• Email: Purchase_orders@ambuUSA.com
• Phone: +1(410)768-6464
• Email: Purchase_orders@ambuUSA.com
• Phone: +1(410)768-6464
• Email: Purchase_orders@ambuUSA.com
• Phone: +1(410)768-6464
• Email: Purchase_orders@ambuUSA.com
• Phone: +1(410)768-6464
• Email: Purchase_orders@ambuUSA.com
• Phone: +1(410)768-6464
• Email: Purchase_orders@ambuUSA.com
• Phone: +1(410)768-6464
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00612649214870 [Package]; Contains: 00612649214887; Package: [30 Units]; In Commercial Distribution
GS1	00612649214887 [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: 2026-01-30
• Device Publish Date: 2022-12-13

On-Brand Devices [ADULT ULTRA FLEX®]

• 00612649214696: ADULT ULTRAFLEX CIRCUIT
• 00612649215129: ADULT ULTRAFLEX CIRCUIT
• 00612649141596: ADULT ULTRAFLEX CIRCUIT
• 00612649158754: ADULT ULTRAFLEX CIRCUIT
• 00612649148861: ADULT ULTRAFLEX CIRCUIT
• 00612649172583: ADULT ULTRAFLEX CIRCUIT
• 00612649158723: ADULT ULTRAFLEX CIRCUIT
• 00612649170282: ADULT ULTRAFLEX CIRCUIT
• 00612649135717: ADULT ULTRAFLEX CIRCUIT
• 00612649215631: ADULT ULTRAFLEX CIRCUIT
• 00612649215617: ADULT ULTRAFLEX CIRCUIT
• 00612649215679: ADULT ULTRA FLEX CIRCUIT PACK KIT
• 00612649215587: ADULT ULTRAFLEX PACK KIT
• 00612649215501: ADULT ULTRAFLEX CIRCUIT
• 00612649215938: ADULT ULTRAFLEX CIRCUIT
• 00612649215761: ADULT ULTRAFLEX CIRCUIT
• 00612649215976: ADULT ULTRAFLEX CIRCUIT
• 00612649215952: ADULT ULTRAFLEX CIRCUIT
• 00612649216249: ADULT ULTRAFLEX CIRCUIT
• 00612649214870: ADULT ULTRAFLEX CIRCUIT
• 00612649170367: ADULT ULTRAFLEX CIRCUIT
• 00612649214801: ADULT ULTRAFLEX CIRCUIT
• 00612649136592: ADULT ULTRAFLEX CIRCUIT
• 00612649161365: ADULT ULTRAFLEX CIRCUIT