Merit PAK™ PAKPHR47NPD4

GUDID 20884450275560

Merit Medical Systems, Inc.

Vascular dilator, single-use

• Primary Device ID: 20884450275560
• NIH Device Record Key: b94a0f7f-456d-4051-90ce-24cdce4777a3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Merit PAK™
• Version Model Number: 10884450275563
• Catalog Number: PAKPHR47NPD4
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 5
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450275566 [Unit of Use]
GS1	10884450275563 [Primary]
GS1	20884450275560 [Package]; Contains: 10884450275563; Package: [4 Units]; In Commercial Distribution

FDA Product Code

• DYB: INTRODUCER, CATHETER

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-10-11
• Device Publish Date: 2016-09-24

On-Brand Devices [Merit PAK™]

• 10884450275716: 00884450275719
• 10884450275693: 00884450275696
• 10884450275624: 00884450275627
• 10884450275686: 00884450275689
• 10884450275662: 00884450275665
• 10884450275723: 00884450275726
• 10884450275730: 00884450275733
• 20884450275577: 10884450275570
• 20884450275560: 10884450275563
• 10884450587130: 00884450587133
• 10884450587147: 00884450587140
• 10884450587123: 00884450587126
• 10884450587192: 00884450587195
• 10884450587178: 00884450587171
• 10884450587154: 00884450587157
• 10884450587161: 00884450587164
• 10884450587185: B