ArcCHECK Cavity Plug 1220000-1Z

GUDID 05060608880157

Accessory to Models 1220 ArcCHECK and 1220-MR ArcCHECK-MR.

SUN NUCLEAR CORP.

Accelerator system quality assurance device

• Primary Device ID: 05060608880157
• NIH Device Record Key: f1df8d22-81d8-4940-84f7-36fcb9c67867
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ArcCHECK Cavity Plug
• Version Model Number: 12200001Z
• Catalog Number: 1220000-1Z
• Company DUNS: 122240021
• Company Name: SUN NUCLEAR CORP.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060608880157 [Primary]
HIBCC	B01612200001Z0 [Previous]

FDA Product Code

• LHO: Instrument, Quality-Assurance, Radiologic

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: 2019-04-12
• Device Publish Date: 2019-04-04

On-Brand Devices [ArcCHECK Cavity Plug]

• B01612200001Z0: Accessory to Models 1220 ArcCHECK and 1220-MR ArcCHECK-MR.
• 05060608880157: Accessory to Models 1220 ArcCHECK and 1220-MR ArcCHECK-MR.