ArcCHECK Cavity Plug 12200001Z

GUDID B01612200001Z0

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

SUN NUCLEAR CORP.

Accelerator system quality assurance device

• Primary Device ID: B01612200001Z0
• NIH Device Record Key: d5c5ec64-235d-4bc5-b4b5-5f3c780fe6a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ArcCHECK Cavity Plug
• Version Model Number: 12200001Z
• Catalog Number: 12200001Z
• 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
HIBCC	B01612200001Z0 [Primary]

FDA Product Code

• LHO: Instrument, Quality-Assurance, Radiologic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-04-17
• Device Publish Date: 2017-01-14

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.