VITA 5002500016

GUDID 18033718001082

250 mL VITA EVA

HAEMOTRONIC SPA

Intravenous administration bag/bottle

• Primary Device ID: 18033718001082
• NIH Device Record Key: d8fee8a3-8ec4-41d5-8bfb-09ae71e321bd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VITA
• Version Model Number: VITA2003R
• Catalog Number: 5002500016
• Company DUNS: 430857771
• Company Name: HAEMOTRONIC SPA
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08033718001085 [Primary]
GS1	18033718001082 [Package]; Contains: 08033718001085; Package: [50 Units]; In Commercial Distribution

FDA Product Code

• KPE: Container, I.V.

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: 2022-04-04
• Device Publish Date: 2022-03-25

On-Brand Devices [VITA]

• 18033718001082: 250 mL VITA EVA
• 18033718001075: 100 mL VITA EVA
• 18033718001068: 50 mL VITA EVA