Y-Cable Top/Bottom Array 3T SI 815053

GUDID 04251269203749

Noras MRI products GmbH

Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal

• Primary Device ID: 04251269203749
• NIH Device Record Key: fd48ccb5-3f59-4b6f-a21d-0582bcf9b4f5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Y-Cable Top/Bottom Array 3T SI
• Version Model Number: 02
• Catalog Number: 815053
• Company DUNS: 312844095
• Company Name: Noras MRI products GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• 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: 0049299270
• Email: sales@noras.de

Device Identifiers

Device Issuing Agency	Device ID
GS1	04251269203749 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K091546

FDA Product Code

• MOS: Coil, Magnetic Resonance, Specialty

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: 2018-08-13
• Device Publish Date: 2018-07-13

On-Brand Devices [Y-Cable Top/Bottom Array 3T SI]

• 04251269203749: 02
• 04251269202629: 02