Active Anthrax Detect Plus Rapid Test

Basic Information

• Brand Name: Active Anthrax Detect Plus Rapid Test
• Primary DI: B379AAP11
• Version / Model: AAP-1
• Company Name: INBIOS INTERNATIONAL, INC
• Labeler DUNS: 004006628
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2023-03-03
• Public Version: 1
• Public Version Date: 2023-03-13
• Public Version Status: New
• Public Device Record Key: cb4547db-8be5-4d2e-8ae5-b90a51e6b6ba

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: Yes
• 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
QUU	Lateral Flow Immunoassay For Protein Detection And Identification Of Bacillus Anthracis	Microbiology	866.3046	2

GMDN Terms

Code	Name	Definition	Implantable	Status
50428	Bacillus anthracis antigen IVD, kit, rapid ICT, clinical	A collection of reagents and other associated materials intended to be used for the qualitative and/or (semi-)quantitative detection of antigens from Bacillus anthracis in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method [lateral flow test]. This is a rapid test used in the laboratory or in point-of-care analyses to detect Bacillus anthracis, the bacteria associated with anthrax. It is not intended to be used for self-testing.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	B379AAP11	HIBCC