Radiolucent Rod Holder LV01299

GUDID 00880304865808

RADIOLUCENT ROD HOLDER

Highridge Medical, LLC

General internal orthopaedic fixation system implantation kit

• Primary Device ID: 00880304865808
• NIH Device Record Key: fe670078-3882-4f95-b5a2-149a10fbd5cf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Radiolucent Rod Holder
• Version Model Number: LV01299
• Catalog Number: LV01299
• 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
• Phone: +1(800)447-3625
• Email: usbrocustomerservice@highridgemedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304865808 [Primary]

FDA Product Code

• GEN: FORCEPS, GENERAL & PLASTIC SURGERY

Sterilization

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

[00880304865808]

Moist Heat or Steam Sterilization

[00880304865808]

Moist Heat or Steam Sterilization

[00880304865808]

Moist Heat or Steam Sterilization

[00880304865808]

Moist Heat or Steam Sterilization

[00880304865808]

Moist Heat or Steam Sterilization

[00880304865808]

Moist Heat or Steam Sterilization

[00880304865808]

Moist Heat or Steam Sterilization

[00880304865808]

Moist Heat or Steam Sterilization

[00880304865808]

Moist Heat or Steam Sterilization

[00880304865808]

Moist Heat or Steam Sterilization

[00880304865808]

Moist Heat or Steam Sterilization

[00880304865808]

Moist Heat or Steam Sterilization

[00880304865808]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-18
• Device Publish Date: 2025-06-10

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• 03662663082051 - ActivL: 2026-02-11 INF PLATE SIZE XL 0DEG SPIKES
• 03662663082068 - ActivL: 2026-02-11 SUP PLATE SIZE XL 6DEG SPIKES
• 03662663082075 - ActivL: 2026-02-11 SUP PLATE SZ XL 11DEG SPIKES
• 03662663082082 - ActivL: 2026-02-11 INF PLATE SIZE XL 0DEG KEEL
• 03662663082099 - ActivL: 2026-02-11 SUP PLATE SIZE XL 6DEG KEEL
• 03662663082105 - ActivL: 2026-02-11 SUP PLATE SIZE XL 11DEG KEEL