NBAC 3.0T SMS, Spine

GUDID 04260486610209

No description.

LMT Medical Systems GmbH

MRI system coil, radio-frequency

• Primary Device ID: 04260486610209
• NIH Device Record Key: 17f92da1-2121-4d12-b428-e95f655cecbc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NBAC 3.0T SMS, Spine
• Version Model Number: 0800143
• Company DUNS: 312688686
• Company Name: LMT Medical Systems GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com
• Phone: +49451580980
• Email: info@lmt-medicalsystems.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260486610209 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K091047

FDA Product Code

• MOS: Coil, Magnetic Resonance, Specialty

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: 2020-03-05
• Device Publish Date: 2018-03-14

On-Brand Devices [NBAC 3.0T SMS, Spine]

• 04260486610209: No description.
• 04260486610636: No description.