IMMY

Basic Information

• Brand Name: IMMY
• Primary DI: 00816387020919
• Version / Model: CR2003
• Company Name: Immuno-Mycologics, Inc.
• Labeler DUNS: 099550915
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 50
• Record Status: Published
• Publish Date: 2016-09-24
• Public Version: 3
• Public Version Date: 2022-03-28
• Public Version Status: Update
• Public Device Record Key: 0dd27dc3-8b2d-4d66-a54d-f8f5d9880d6b

Device Description

Cryptococcal Antigen Lateral Flow Assay

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
GMD	Antisera, Latex Agglutination, Cryptococcus Neoformans	Microbiology	866.3165	2

GMDN Terms

Code	Name	Definition	Implantable	Status
52074	Cryptococcus neoformans antigen IVD, reagent	A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of antigens from the yeast Cryptococcus neoformans in a clinical specimen.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00816387020919	GS1
Unit of Use	00816387020933	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]