Preston™ CD1115/B

GUDID 10884450411800

Merit Medical Systems, Inc.

Bone biopsy needle

• Primary Device ID: 10884450411800
• NIH Device Record Key: b40bb558-7a37-4b99-8b29-d4d3795a522b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Preston™
• Version Model Number: 00884450411803
• Catalog Number: CD1115/B
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450411803 [Primary]
GS1	10884450411800 [Package]; Contains: 00884450411803; Package: [14 Units]; In Commercial Distribution

FDA Product Code

• DWO: NEEDLE, BIOPSY, CARDIOVASCULAR

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-11-20
• Device Publish Date: 2019-11-12

On-Brand Devices [Preston™]

• 20884450412064: 10884450412067
• 10884450411794: 00884450411797
• 10884450411800: 00884450411803
• 10884450411756: 00884450411759
• 10884450412012: 00884450412015
• 10884450411763: 00884450411766
• 10884450411787: 00884450411780
• 10884450412005: 00884450412008