ALIF

GUDID 00841732166899

ALIF Wedge Distractor Tip Caddy

CTL Medical Corporation

Device sterilization/disinfection container, reusable

• Primary Device ID: 00841732166899
• NIH Device Record Key: 6d5cd147-2ebe-411c-ac8b-5fe21730a668
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ALIF
• Version Model Number: 106.8074
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841732166899 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K192863

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

[00841732166899]

Moist Heat or Steam Sterilization

[00841732166899]

Moist Heat or Steam Sterilization

[00841732166899]

Moist Heat or Steam Sterilization

[00841732166899]

Moist Heat or Steam Sterilization

[00841732166899]

Moist Heat or Steam Sterilization

[00841732166899]

Moist Heat or Steam Sterilization

[00841732166899]

Moist Heat or Steam Sterilization

[00841732166899]

Moist Heat or Steam Sterilization

[00841732166899]

Moist Heat or Steam Sterilization

[00841732166899]

Moist Heat or Steam Sterilization

[00841732166899]

Moist Heat or Steam Sterilization

[00841732166899]

Moist Heat or Steam Sterilization

[00841732166899]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-11
• Device Publish Date: 2024-11-01

Devices Manufactured by CTL Medical Corporation

• 00841732146181 - SEURAT: 2025-04-09 SEURAT Screw Body, HEX4.0, D4.5xL60mm
• 00841732146198 - SEURAT: 2025-04-09 SEURAT Screw Body, HEX4.0, D5.0xL25mm
• 00841732146204 - SEURAT: 2025-04-09 SEURAT Screw Body, HEX4.0, D5.0xL30mm
• 00841732146211 - SEURAT: 2025-04-09 SEURAT Screw Body, HEX4.0, D5.0xL35mm
• 00841732146228 - SEURAT: 2025-04-09 SEURAT Screw Body, HEX4.0, D5.0xL40mm
• 00841732146235 - SEURAT: 2025-04-09 SEURAT Screw Body, HEX4.0, D5.0xL45mm
• 00841732146242 - SEURAT: 2025-04-09 SEURAT Screw Body, HEX4.0, D5.0xL50mm
• 00841732146259 - SEURAT: 2025-04-09 SEURAT Screw Body, HEX4.0, D5.0xL55mm