Monet ACIF

GUDID 00841732165793

ACIF Trial, SM, Lordotic, H7/H8mm

CTL Medical Corporation

Spinal implant trial

• Primary Device ID: 00841732165793
• NIH Device Record Key: 5ba45a59-5151-4d1c-8b9a-d18dc2e1392d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Monet ACIF
• Version Model Number: 113.7317
• Company DUNS: 080138504
• Company Name: CTL Medical Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com
• Phone: 214-545-5820
• Email: schedule@ctlamedica.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841732165793 [Primary]

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

[00841732165793]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-12-04
• Device Publish Date: 2024-11-26

On-Brand Devices [Monet ACIF]

• 00841732165830: ACIF Trial, MD, Lordotic, H9/H10mm
• 00841732165823: ACIF Trial, MD, Lordotic, H7/H8mm
• 00841732165816: ACIF Trial, MD, Lordotic, H5/H6mm
• 00841732165809: ACIF Trial, SM, Lordotic, H9/H10mm
• 00841732165793: ACIF Trial, SM, Lordotic, H7/H8mm
• 00841732165786: ACIF Trial, SM, Lordotic, H5/H6mm