Nimbus

GUDID 00195377055538

Nimbus Adapter, Large Clamp

Nuvasive, Inc.

Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system

• Primary Device ID: 00195377055538
• NIH Device Record Key: 99df9aca-91c6-47cd-a2d1-7db30f99841d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nimbus
• Version Model Number: 6973332
• Company DUNS: 053950783
• Company Name: Nuvasive, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00195377055538 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

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

[00195377055538]

Moist Heat or Steam Sterilization

[00195377055538]

Moist Heat or Steam Sterilization

[00195377055538]

Moist Heat or Steam Sterilization

[00195377055538]

Moist Heat or Steam Sterilization

[00195377055538]

Moist Heat or Steam Sterilization

[00195377055538]

Moist Heat or Steam Sterilization

[00195377055538]

Moist Heat or Steam Sterilization

[00195377055538]

Moist Heat or Steam Sterilization

[00195377055538]

Moist Heat or Steam Sterilization

[00195377055538]

Moist Heat or Steam Sterilization

[00195377055538]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-01
• Device Publish Date: 2024-04-23

On-Brand Devices [Nimbus]

• 00195377061232: Nimbus Adapters Tray
• 00195377055552: Nimbus Adapter, Small Clamp
• 00195377055545: Nimbus Adapter, Medium Clamp
• 00195377055538: Nimbus Adapter, Large Clamp
• 00195377055521: Maxcess Adapter, A-Arm Threaded