ArcCHECK PMMA MultiPlug 1220000-3Z

GUDID 05060608880164

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

SUN NUCLEAR CORP.

Accelerator system quality assurance device

• Primary Device ID: 05060608880164
• NIH Device Record Key: e4a881ee-a6df-4b0d-862a-76ddde3925ed
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ArcCHECK PMMA MultiPlug
• Version Model Number: 1220000-3Z
• Catalog Number: 1220000-3Z
• 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

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store the ArcCHECK, ancillary parts, and accessories in an indoor, climate-controlled environment consistent with specified environmental conditions

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060608880164 [Primary]
HIBCC	B01612200003Z0 [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: 2019-10-09
• Device Publish Date: 2019-10-01

On-Brand Devices [ArcCHECK PMMA MultiPlug]

• B01612200003Z0: Accessory to Models 1220 ArcCHECK and 1220-MR ArcCHECK-MR.
• 05060608880164: Accessory to Models 1220 ArcCHECK and 1220-MR ArcCHECK-MR.