G-MOPS

GUDID 07350025910819

Vitrolife Sweden AB

IVF medium

• Primary Device ID: 07350025910819
• NIH Device Record Key: c3bd8a7a-b5ff-4a29-89f2-6fa33100c519
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: G-MOPS
• Version Model Number: 10181
• Company DUNS: 631805488
• Company Name: Vitrolife Sweden AB
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07350025910819 [Primary]

FDA Product Code

• MQL: Media, Reproductive

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: 2021-06-04
• Device Publish Date: 2021-05-27

On-Brand Devices [G-MOPS]

• 07350025910468: 10129
• 07350025910819: 10181