Corning

GUDID H10840215CV1

MEDIATECH, INC.

Blood/tissue storage/culture container

• Primary Device ID: H10840215CV1
• NIH Device Record Key: 20508c24-d711-481d-9f18-915d7897f0fa
• Commercial Distribution Discontinuation: 2023-04-05
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Corning
• Version Model Number: 40-215-CV
• Company DUNS: 181302050
• Company Name: MEDIATECH, INC.
• Device Count: 6
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	H10840215CV0 [Unit of Use]
HIBCC	H10840215CV1 [Primary]

FDA Product Code

• KIT: MEDIA AND COMPONENTS, SYNTHETIC CELL AND TISSUE CULTURE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2023-04-06
• Device Publish Date: 2020-12-04

On-Brand Devices [Corning]

• H10840215CV3: Corning® 500 mL hybrigro SF™
• H10820021CV3: Corning® 500 mL HBSS (Hanks Balanced Salt Solution), 10x [-] sodium bicarbonate, calcium, magne
• H10840215CV1: 40-215-CV
• H10820021CV1: 20-021-CV