SPECTRALINE™ 622601

GUDID 20884450671614

Merit Medical Systems, Inc.

General-purpose syringe, single-use

• Primary Device ID: 20884450671614
• NIH Device Record Key: 9aea2199-9ae9-4e4f-a2a8-97437070a1fa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SPECTRALINE™
• Version Model Number: 00884450671610
• Catalog Number: 622601
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450671610 [Primary]
GS1	10884450671617 [Package]; Contains: 00884450671610; Package: [25 Units]; In Commercial Distribution
GS1	20884450671614 [Package]; Contains: 10884450671617; Package: [4 Units]; In Commercial Distribution

FDA Product Code

• FMF: Syringe, piston

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: 2025-07-28
• Device Publish Date: 2025-07-18

On-Brand Devices [SPECTRALINE™]

• 10884450671662: 00884450671665
• 20884450671652: 00884450671658
• 10884450671648: 00884450671641
• 10884450671631: 00884450671634
• 20884450671614: 00884450671610
• 10884450671600: 00884450671603
• 20884450671690: 00884450671696
• 20884450671683: 00884450671689
• 20884450671676: 00884450671672