ArcCHECK PMMA MultiPlug 12200003Z

GUDID B01612200003Z0

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

SUN NUCLEAR CORP.

Accelerator system quality assurance device

• Primary Device ID: B01612200003Z0
• NIH Device Record Key: 6df28978-53a8-4514-87b7-4c81c83b877f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ArcCHECK PMMA MultiPlug
• Version Model Number: 12200003Z
• Catalog Number: 12200003Z
• 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	B01612200003Z0 [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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-01-14

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.