NBAC 3.0T SMS, Flex

GUDID 04260486610216

No description.

LMT Medical Systems GmbH

MRI system coil, radio-frequency

• Primary Device ID: 04260486610216
• NIH Device Record Key: 05ed7df1-75ab-40d2-b429-eeb2a38a42dd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NBAC 3.0T SMS, Flex
• Version Model Number: 0800144
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260486610216 [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

Devices Manufactured by LMT Medical Systems GmbH

• 04260486610483 - NHAC 1.5T PH I 16: 2024-05-01 No description.
• 04260486610537 - NHAC 3.0T PH I 16: 2024-05-01 No description.
• 04260486610582 - NBAC 1.5T PH I Spine: 2024-05-01 No description.
• 04260486610599 - NBAC 3.0T PH I Spine: 2024-05-01 No description.
• 04260486610940 - NBAC 1.5T SMS, Flex: 2023-06-09 No description.
• 04260486610957 - NBAC 1.5T PH I Flex: 2023-06-09 No description.
• 04260486610377 - NBAC 3.0T GE H, Flex: 2022-02-22 No description.
• 04260486610544 - NHAC 3.0T GE P 16: 2022-02-22 No description.