Jumbo

GUDID 00817051021942

JUMBO TUBE STARTER KIT

CENTRIX, INC.

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• Primary Device ID: 00817051021942
• NIH Device Record Key: ee76efc5-3d3f-4848-b2d1-f49ed1e64153
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Jumbo
• Version Model Number: 180615
• Company DUNS: 053707303
• Company Name: CENTRIX, 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: true
• 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	00817051021942 [Primary]

FDA Product Code

• EID: Syringe, Restorative And Impression Material

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-08
• Device Publish Date: 2023-12-29

On-Brand Devices [Jumbo]

• 00817051022307: JUMBO TUBES
• 00817051021942: JUMBO TUBE STARTER KIT