MB9076R MB9074R

GUDID 03662663001472

LDR Spine Usa, Inc.

Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps 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

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

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