MB9076R MB9074R

GUDID 03662663001472

LDR Spine Usa, Inc.

Bone distraction forceps

• Primary Device ID: 03662663001472
• NIH Device Record Key: 31ab9da1-5f54-4732-940b-2f3b49280d44
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MB9076R
• Version Model Number: MB9076R
• Catalog Number: MB9074R
• 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

Customer Support Contacts

• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com
• Phone: 800-699-3360
• Email: custserv@ldrspine.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	03662663001472 [Primary]

FDA Product Code

• GEN: Forceps, General & Plastic Surgery

Sterilization

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

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

[03662663001472]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2022-03-10
• Device Publish Date: 2018-12-12

Devices Manufactured by LDR Spine Usa, Inc.

• 03662663059169 - Mobi-C Plug & Fit US: 2024-01-23 Trial Implant Holder with Depth Stop
• 03662663059176 - Mobi-C Plug & Fit US: 2024-01-23 Reinforced Rigid Distraction Forceps
• 03662663059183 - Mobi-C Plug & Fit US: 2024-01-23 Reinforced Rigid Distraction Forceps
• 03662663059145 - Mobi-C Plug & Fit US: 2024-01-22 Reinforced Distraction Forceps
• 03662663059152 - Mobi-C Plug & Fit US: 2024-01-22 Slim Mobi-C No Touch Implant Holder
• 03662663000215 - Mobi-C: 2022-03-10
• 03662663000222 - Mobi-C: 2022-03-10
• 03662663000239 - Mobi-C: 2022-03-10