CleanCut Rotating Aortic Punch Bulk Nonsterile RCL50BNS

GUDID 20634624375028

QUEST MEDICAL INC

Aorta punch, single-use

• Primary Device ID: 20634624375028
• NIH Device Record Key: af360eb4-e886-4fac-8a91-9874249a6d40
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CleanCut Rotating Aortic Punch Bulk Nonsterile
• Version Model Number: RCL50BNS
• Catalog Number: RCL50BNS
• Company DUNS: 041810693
• Company Name: QUEST MEDICAL INC
• Device Count: 50
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	00634624375024 [Unit of Use]
GS1	20634624375028 [Primary]

FDA Product Code

• DWS: Instruments, Surgical, Cardiovascular

Sterilization

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

[20634624375028]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-11-13
• Device Publish Date: 2019-10-10

On-Brand Devices [CleanCut Rotating Aortic Punch Bulk Nonsterile]

• 20634624375028: RCL50BNS
• 20634624374823: RCL48BNS
• 20634624374021: RCL40BNS