Pre-Filled Saline Flush Syringe,Sterile,5mL

GUDID 00840117334489

DYNAREX CORPORATION

Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial

• Primary Device ID: 00840117334489
• NIH Device Record Key: fffe1625-bb36-4550-8f97-56eff38f0cd4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pre-Filled Saline Flush Syringe,Sterile,5mL
• Version Model Number: 7058
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• Device Count: 30
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840117334489 [Package]; Contains: 00840117334496; Package: Case [16 Units]; In Commercial Distribution
GS1	00840117334496 [Primary]
GS1	00840117334502 [Unit of Use]
GS1	08401173344960 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K220060

FDA Product Code

• NGT: Saline, Vascular Access Flush

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: 2024-03-15
• Device Publish Date: 2024-03-07

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