HLX Transducer

GUDID 04068151010022

SIEMENS MEDICAL SOLUTIONS USA, INC.

Extracorporeal ultrasound imaging transducer, hand-held

• Primary Device ID: 04068151010022
• NIH Device Record Key: 68706a11-6056-4428-9b4d-97ed45747cb7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HLX Transducer
• Version Model Number: 11575216
• Company DUNS: 804722783
• Company Name: SIEMENS MEDICAL SOLUTIONS USA, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• 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: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM
• Phone: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM
• Phone: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM
• Phone: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM
• Phone: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM
• Phone: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM
• Phone: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM
• Phone: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM
• Phone: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM
• Phone: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM
• Phone: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM
• Phone: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM
• Phone: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM
• Phone: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM
• Phone: +1(800)888-7436
• Email: CONTACT@SIEMENS-HEALTHINEERS.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	04068151010022 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K242523

FDA Product Code

• ITX: Transducer, ultrasonic, diagnostic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-12-05
• Device Publish Date: 2024-11-27

Devices Manufactured by SIEMENS MEDICAL SOLUTIONS USA, INC.

• 04056869990415 - 11M2 Transducer: 2024-12-05
• 04068151010022 - HLX Transducer: 2024-12-05
• 04068151010022 - HLX Transducer: 2024-12-05
• 04068151009477 - Scenium: 2024-09-16
• 04068151027013 - MI View&GO: 2024-09-16
• 04068151012477 - ACUSON Origin ICE Diagnostic Ultrasound System: 2024-08-30
• 04056869997445 - AcuNav Lumos 4D ICE catheter: 2024-07-29
• 04068151001303 - ACUSON P500 ICE Ultrasound System: 2024-07-09
• 04056869950747 - 6C1 HD Transducer: 2024-05-16