Kallestad Crithidia luciliae 8 Well Slides
Kallestad - 26110
Device Description
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 antibodies to native DNA (anti-nDNA) in a clinical specimen.
Environmental Conditions
- -20.00
- -20.00
Device Sizes
- 160 Tests
- 8 Wells
Device Sterilization
Device Sterile: False
Sterilization Prior To Use: False
Sterilization Methods: No Data Available
Product Codes
Code: DHN
Device Name: Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
Device Class: 2
Physical State: N/A
Definition: N/A
Submission Type ID: 1
Review Panel: IM
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: N/A
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: N
Target Area: N/A
Regulation Number: 866.5100
Third Party Flag: Y
Medical Specialty: IM
Device IdentifiersDevice Id: 00847865001571
Device Type: Primary
DeviceId Issuing Agency: GS1
Contains DI Number: N/A
Package Quantity: N/A
Package Discontinue Date: N/A
Package Status: N/A
Package Type: N/A