FDA UDI In Commercial Distribution 🇺🇸 United States

ANA Detect ELISA

DI: 00840239041173 · Model: EIA-4117 · DRG International Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ANA Detect ELISA
Primary DI
00840239041173
Version / Model
EIA-4117
Catalog Number
EIA-4117
Company Name
DRG International Inc
Labeler DUNS
075150847
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-25
Public Version
2
Public Version Date
2026-02-09
Public Version Status
Update
Public Device Record Key
d192a5b1-d977-424f-b05f-bcd6e6e9a82b

Device Description

ANA Detect ELISA is a test system for the qualitative measurement of IgG class autoantibodies against SS-A-52 (Ro 52), SS-A-60 (Ro-60), SS-B (La), RNP/Sm, RNP-70, RNP-A, RNP-C, Sm-BB, Sm-D, Sm-E, Sm-F, Sm-G, Scl-70, Jo-1, dsDNA, ssDNA, polynucleosomes, mononucleosomes, histone complex, histone H1, histone H2A, histone H2B, histone 3, histone H4, Pm-Scl-100 and centromere B in human serum or plasma samples.

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LJM Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls

GMDN Terms

Code Name
54809 Multiple antinuclear antibody (ANA) IVD, kit, enzyme immunoassay (EIA)

Identifiers

Type ID
Primary 00840239041173

Customer Contacts

Phone
9735647555

Premarket Submissions

Submission Number Supplement Number
K030929 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius