Cultura™ C100F/B

GUDID 20884450495845

Merit Medical Systems, Inc.

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• Primary Device ID: 20884450495845
• NIH Device Record Key: c2e24aca-6eae-4da1-abfd-1c4dc0b5f896
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cultura™
• Version Model Number: 00884450495841
• Catalog Number: C100F/B
• 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	00884450495841 [Primary]
GS1	10884450495848 [Package]; Contains: 00884450495841; Package: [75 Units]; In Commercial Distribution
GS1	20884450495845 [Package]; Contains: 10884450495848; 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: 2020-07-08
• Device Publish Date: 2020-06-30

On-Brand Devices [Cultura™]

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