CleanCut Rotating Aortic Punch, 3.5 mm Nonsterile RCL35BNS

GUDID 20634624373529

QUEST MEDICAL INC

Aorta punch, single-use

• Primary Device ID: 20634624373529
• NIH Device Record Key: fca5a70e-fc0f-4731-8f68-a117344cc6ac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CleanCut Rotating Aortic Punch, 3.5 mm Nonsterile
• Version Model Number: RCL35BNS
• Catalog Number: RCL35BNS
• 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	00634624373525 [Unit of Use]
GS1	20634624373529 [Primary]

FDA Product Code

• DWS: Instruments, Surgical, Cardiovascular

Sterilization

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

[20634624373529]

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, 3.5 mm Nonsterile]

• 20634624373529: RCL35BNS
• 20634624333523: .