CleanCut 5.0 mm Nonsterile Aortic Punch RCC50BNS

GUDID 20634624335022

.

QUEST MEDICAL INC

Aorta punch, single-use

• Primary Device ID: 20634624335022
• NIH Device Record Key: ed6c4885-654b-4943-8635-92040ce24be9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CleanCut 5.0 mm Nonsterile Aortic Punch
• Version Model Number: RCC50BNS
• Catalog Number: RCC50BNS
• 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	00634624335028 [Unit of Use]
GS1	20634624335022 [Primary]

FDA Product Code

• DWS: Instruments, Surgical, Cardiovascular

Sterilization

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

[20634624335022]

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

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