Proteus OXK Agglutinating Serum

Basic Information

• Brand Name: Proteus OXK Agglutinating Serum
• Primary DI: 05056080501611
• Version / Model: R30165901
• Company Name: REMEL EUROPE LIMITED
• Labeler DUNS: 232600853
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2021-07-21
• Public Version: 1
• Public Version Date: 2021-07-29
• Public Version Status: New
• Public Device Record Key: 62f0a181-4dbd-4b5a-a948-4feb8843e17a

Device Characteristics

• Single Use: No
• Prescription Use (Rx): No
• 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: Yes
• 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
GSY	Antisera, Fluorescent, All Globulins, Proteus Spp.	Microbiology	866.3410	1

GMDN Terms

Code	Name	Definition	Implantable	Status
51300	Multiple Rickettsia species (spotted fever group) total antibody IVD, control	A material which is used to verify the performance of an assay intended to be used for the qualitative and/or quantitative detection of total antibodies to one or multiple species of the rickettsial bacteria associated with spotted fever in a clinical specimen. Rickettsia species intended to be detected may include Rickettsia rickettsii, R. akari, R. conorii, R. sibirica, R. australis, R. japonica, R. africae, R. honei and/or R. felis.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	05056080501611	GS1

Customer Contacts

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