DBX® 048125

GUDID W4184048125T0479

DBX Strip Trauma 2.5cm x 5cm

Musculoskeletal Transplant Foundation, Inc.

Bone matrix implant, human-derived

• Primary Device ID: W4184048125T0479
• NIH Device Record Key: 74502214-3438-4e10-b209-4f202a88bdd5
• Commercial Distribution Discontinuation: 2019-06-12
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: DBX®
• Version Model Number: 048125
• Catalog Number: 048125
• Company DUNS: 187560545
• Company Name: Musculoskeletal Transplant Foundation, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: true
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 800-433-6576
• Email: RA_Licenses@mtf.org

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
ICCBBA	W4184048125T0479 [Primary]

FDA Product Code

• MBP: Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-06-13
• Device Publish Date: 2016-02-19

On-Brand Devices [DBX®]

• W4184048125T0479: DBX Strip Trauma 2.5cm x 5cm
• W4184048050T0479: DBX Strip 5cm x 5cm
• W4184048025T0479: DBX Strip 2.5cm x 5cm
• W4184048015T0479: DBX Strip 1.5cm x 1.5cm
• W4184048010T0479: DBX Strip 2.5cm x 10cm