Rampart

GUDID 00860002090108

Radiation Shielding Panel, portal/mobile

Rampart Ic, LLC

Radiation shielding panel, portable/mobile

• Primary Device ID: 00860002090108
• NIH Device Record Key: 2b791511-6cfc-4ffc-9b50-701e91d67894
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rampart
• Version Model Number: M1128-RTV01
• Company DUNS: 117119538
• Company Name: Rampart Ic, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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	00860002090108 [Primary]

FDA Product Code

• EAK: Screen, Leaded, Operator Radiation Protector

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: 2023-09-04
• Device Publish Date: 2023-08-25

On-Brand Devices [Rampart ]

• 00860002090191: Table Mounting Shield
• 00860002090184: Radiation Shield
• 00860002090177: Radiation Shield
• 00860002090108: Radiation Shielding Panel, portal/mobile