High Pressure Tubing, Keep™ HPF721K/A

GUDID 20884450387713

Merit Medical Systems, Inc.

Radiographic procedure tubing

• Primary Device ID: 20884450387713
• NIH Device Record Key: 35cb500e-4ec8-44eb-97dc-44a06e382a1d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: High Pressure Tubing, Keep™
• Version Model Number: 00884450387719
• Catalog Number: HPF721K/A
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• 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 Dimensions

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450387719 [Primary]
GS1	10884450387716 [Package]; Contains: 00884450387719; Package: [25 Units]; In Commercial Distribution
GS1	20884450387713 [Package]; Contains: 10884450387716; Package: [4 Units]; In Commercial Distribution

FDA Product Code

• DXJ: DISPLAY, CATHODE-RAY TUBE, MEDICAL

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: 2022-02-28
• Device Publish Date: 2022-02-18

On-Brand Devices [High Pressure Tubing, Keep™]

• 10884450569167: 00884450569160
• 10884450568634: 00884450568637
• 20884450387713: 00884450387719
• 10884450387693: 00884450387696
• 20884450387638: 00884450387634
• 20884450387676: 00884450387672
• 20884450387669: 00884450387665
• 10884450568658: 00884450568651
• 10884450568702: 00884450568705
• 20884450387553: 00884450387559
• 20884450807112: C
• 20884450821262: B