Mobi-C Plug & Fit US

GUDID 03662663059169

Trial Implant Holder with Depth Stop

LDR Spine Usa, Inc.

Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable

• Primary Device ID: 03662663059169
• NIH Device Record Key: 098dd2bb-57c2-4553-8d76-92fac2f869d2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mobi-C Plug & Fit US
• Version Model Number: MB9117R
• Company DUNS: 615789729
• Company Name: LDR Spine Usa, 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	03662663059169 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

[03662663059169]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-23
• Device Publish Date: 2024-01-15

On-Brand Devices [Mobi-C Plug & Fit US]

• 03662663059152: Slim Mobi-C No Touch Implant Holder
• 03662663059145: Reinforced Distraction Forceps
• 03662663059183: Reinforced Rigid Distraction Forceps
• 03662663059176: Reinforced Rigid Distraction Forceps
• 03662663059169: Trial Implant Holder with Depth Stop