Excite™ HPC390E

GUDID 20884450021419

Merit Medical Systems, Inc.

Radiographic procedure tubing

• Primary Device ID: 20884450021419
• NIH Device Record Key: 59c2cc2b-f949-499d-9173-9094833a5499
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Excite™
• Version Model Number: 00884450021415
• Catalog Number: HPC390E
• 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

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450021415 [Primary]
GS1	10884450021412 [Package]; Contains: 00884450021415; Package: [25 Units]; In Commercial Distribution
GS1	20884450021419 [Package]; Contains: 10884450021412; Package: [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K883718

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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

On-Brand Devices [Excite™]

• 10884450381004: 00884450381007
• 10884450380991: 00884450380994
• 20884450380981: 00884450380987
• 10884450380977: 00884450380970
• 20884450380950: 00884450380956
• 10884450380939: 00884450380932
• 20884450380912: 00884450380918
• 10884450380892: 00884450380895
• 10884450380885: 00884450380888
• 10884450380878: 00884450380871
• 20884450105256: 00884450105252
• 10884450104344: 00884450104347
• 10884450030346: 00884450030349
• 10884450029234: 00884450029237
• 20884450027947: 00884450027943
• 10884450027933: 00884450027936
• 10884450027926: 00884450027929
• 10884450025663: 00884450025666
• 20884450024267: 00884450024263
• 10884450021429: 00884450021422
• 20884450021419: 00884450021415
• 20884450021402: 00884450021408
• 10884450011437: 00884450011430
• 20884450008571: 00884450008577
• 10884450380946: 00884450380949
• 20884450380929: 00884450380925
• 20884450380905: 00884450380901