MEDRAD® MRXperion MR Injection System SSMR START

GUDID 00616258008165

"Hand switch with mounting hardware (85276557)"

BAYER MEDICAL CARE INC.

Contrast medium injection system hand controller kit

• Primary Device ID: 00616258008165
• NIH Device Record Key: ddd7343d-8478-42d1-a9ec-db67d5ec3bbd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MEDRAD® MRXperion MR Injection System
• Version Model Number: SSMR START
• Catalog Number: SSMR START
• Company DUNS: 058716649
• Company Name: BAYER MEDICAL CARE INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• 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)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com
• Phone: +1(800)633-7231
• Email: ricustomercomplaints@bayer.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00616258008165 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K143538

FDA Product Code

• DXT: Injector And Syringe, Angiographic

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: 2018-07-06
• Device Publish Date: 2016-09-24

On-Brand Devices [MEDRAD® MRXperion MR Injection System]

• 00616258008165: "Hand switch with mounting hardware (85276557)"
• 00616258008158: "ASSY,POLE,IV,SINGLE HOOK (84284246)"
• 00616258008141: "Assy, IV Pole, MRXperion (84290149)"
• 00616258008134: "SYSTEM,INJECTOR,MRXPERION (84200085)"
• 00616258021355: SYSTEM,INJECTOR,MRXPERION (86410036)
• 00616258025094: SYSTEM,INJECTOR,MRXPERION,CORE,LR (87838420)