Vitrification Media 91103

GUDID 14582231462947

Contains BS x 1, ES x 1, and VS x 2

KITAZATO CORPORATION

IVF medium kit IVF medium kit IVF medium kit IVF medium kit IVF medium kit IVF medium kit IVF medium kit IVF medium kit IVF medium kit IVF medium kit IVF medium kit IVF medium kit IVF medium kit IVF medium kit IVF medium kit IVF medium kit IVF medium kit IVF medium kit

• Primary Device ID: 14582231462947
• NIH Device Record Key: 6b99ecb6-24d8-4f82-8506-a6052ee4154a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vitrification Media
• Version Model Number: VT601US
• Catalog Number: 91103
• Company DUNS: 711091157
• Company Name: KITAZATO CORPORATION
• Device Count: 4
• 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: true
• 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	04582231462957 [Unit of Use]
GS1	14582231462947 [Primary]

FDA Product Code

• MQL: MEDIA, REPRODUCTIVE

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: 2020-01-08
• Device Publish Date: 2018-08-03

On-Brand Devices [Vitrification Media]

• 14582231462947: Contains BS x 1, ES x 1, and VS x 2
• 14582231462596: Contains ES and VS×2