Cultura™ C80F

GUDID 20884450504707

Merit Medical Systems, Inc.

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• Primary Device ID: 20884450504707
• NIH Device Record Key: c9bba08e-029d-41f9-b137-3aa033e5dbb2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cultura™
• Version Model Number: 00884450504703
• Catalog Number: C80F
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 1
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450504703 [Primary]
GS1	10884450504700 [Package]; Contains: 00884450504703; Package: [75 Units]; In Commercial Distribution
GS1	20884450504707 [Package]; Contains: 10884450504700; Package: [4 Units]; In Commercial Distribution

FDA Product Code

• KXG: APPLICATOR, ABSORBENT TIPPED, STERILE

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-08
• Device Publish Date: 2020-08-31

On-Brand Devices [Cultura™]

• 20884450495845: 00884450495841
• 20884450506718: 00884450506714
• 10884450495831: 00884450495834
• 20884450491106: 00884450491102
• 20884450504707: 00884450504703
• 20884450525764: 10884450525767
• 10884450525750: 00884450525753
• 20884450525726: 00884450525722
• 20884450520127: 10884450520120
• 10884450742126: 00884450742129