InFix Anterior Lumbar Device 1898-001-120

GUDID 00887868291531

Implant Template-120 %

Highridge Medical, LLC

Surgical implant template, reusable

• Primary Device ID: 00887868291531
• NIH Device Record Key: 8a10cbec-c87b-4654-ae76-19d93e2b3047
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: InFix Anterior Lumbar Device
• Version Model Number: 1898-001-120
• Catalog Number: 1898-001-120
• Company DUNS: 119260394
• Company Name: Highridge Medical, LLC
• 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: false
• 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: +1(800)447-3625
• Email: usbrocustomerservice@highridgemedical.com
• Phone: +1(800)447-3625
• Email: usbrocustomerservice@highridgemedical.com
• Phone: +1(800)447-3625
• Email: usbrocustomerservice@highridgemedical.com
• Phone: +1(800)447-3625
• Email: usbrocustomerservice@highridgemedical.com
• Phone: +1(800)447-3625
• Email: usbrocustomerservice@highridgemedical.com
• Phone: +1(800)447-3625
• Email: usbrocustomerservice@highridgemedical.com
• Phone: +1(800)447-3625
• Email: usbrocustomerservice@highridgemedical.com
• Phone: +1(800)447-3625
• Email: usbrocustomerservice@highridgemedical.com
• Phone: +1(800)447-3625
• Email: usbrocustomerservice@highridgemedical.com
• Phone: +1(800)447-3625
• Email: usbrocustomerservice@highridgemedical.com
• Phone: +1(800)447-3625
• Email: usbrocustomerservice@highridgemedical.com
• Phone: +1(800)447-3625
• Email: usbrocustomerservice@highridgemedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868291531 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

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

[00887868291531]

Moist Heat or Steam Sterilization

[00887868291531]

Moist Heat or Steam Sterilization

[00887868291531]

Moist Heat or Steam Sterilization

[00887868291531]

Moist Heat or Steam Sterilization

[00887868291531]

Moist Heat or Steam Sterilization

[00887868291531]

Moist Heat or Steam Sterilization

[00887868291531]

Moist Heat or Steam Sterilization

[00887868291531]

Moist Heat or Steam Sterilization

[00887868291531]

Moist Heat or Steam Sterilization

[00887868291531]

Moist Heat or Steam Sterilization

[00887868291531]

Moist Heat or Steam Sterilization

[00887868291531]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-12-26
• Device Publish Date: 2025-12-18

On-Brand Devices [InFix Anterior Lumbar Device]

• 00887868291531: Implant Template-120 %
• 00887868291333: Implant Tray Lid, Small
• 00887868291326: Implant Tray, Small
• 00887868291319: Endcap Tray Lid