N-Force Blue

GUDID 00889024430075

Zimmer, Inc.

Synthetic bone graft

• Primary Device ID: 00889024430075
• NIH Device Record Key: b126ff8a-7cd4-4fc6-8da6-6d9d29512048
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: N-Force Blue
• Version Model Number: IN050-1
• Company DUNS: 056038268
• Company Name: Zimmer, 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: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Total Volume: 10 Milliliter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024430075 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K093447

FDA Product Code

• MQV: Filler, Bone Void, Calcium Compound

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-12-19
• Device Publish Date: 2016-04-29

Devices Manufactured by Zimmer, Inc.

• 00887868585661 - Zimmer Biomet® 12/14 Spherical Head Trials: 2024-11-19
• 00887868139628 - Affixus®: 2024-11-18
• 00887868139635 - Affixus®: 2024-11-18
• 00887868139642 - Affixus®: 2024-11-18
• 00887868139659 - Affixus®: 2024-11-18
• 00887868139666 - Affixus®: 2024-11-18
• 00887868139673 - Affixus®: 2024-11-18
• 00887868139680 - Affixus®: 2024-11-18