IV Start Kit

GUDID 00860008059512

DYNAREX CORPORATION

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• Primary Device ID: 00860008059512
• NIH Device Record Key: 696fd162-fca4-4bc5-8b07-ae209acce55c
• Commercial Distribution Discontinuation: 2024-04-09
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: IV Start Kit
• Version Model Number: 13001
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• Device Count: 50
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860008059512 [Primary]
GS1	00860008123220 [Unit of Use]

FDA Product Code

• OHR: Catheter Care Tray

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-04-10
• Device Publish Date: 2022-01-06

On-Brand Devices [IV Start Kit]

• 00616784469621: IV Start Kit, Stretch Vinyl Gloves, Sterile, 1 Tourniquet (3/4" x 18"), 2 Gauze Sponge (2" x 2
• 00616784469225: IV Start Kit, Sterile, 1 Tourniquet (3/4" x 18"), 2 Gauze Sponge (2" x 2", 8-Ply), 1 ID Label, 1
• 00860008059512: 13001