FDA UDI In Commercial Distribution 🇺🇸 United States

ANCA Screen IgG ELISA

DI: 04048474027778 · Model: EIA-2777 · DRG Instruments Gesellschaft mit beschränkter Haftung
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ANCA Screen IgG ELISA
Primary DI
04048474027778
Version / Model
EIA-2777
Catalog Number
EIA-2777
Company Name
DRG Instruments Gesellschaft mit beschränkter Haftung
Labeler DUNS
317134468
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-29
Public Version
1
Public Version Date
2023-09-06
Public Version Status
New
Public Device Record Key
9b5e5da2-fc3b-4f6c-8bb7-35a4451d570f

Device Description

The ANCA Screen ELISA test system is intended for the qualitative detection of anti-Myeloperoxidase and/or anti-Proteinase-3 IgG antibody in human serum. The test system is intended to be used as an aid in the diagnosis of various autoimmune vasculitic disorders characterized by elevated levels of anti-neutrophil cytoplasmic antibodies (ANCA).

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
MOB Test System, Antineutrophil Cytoplasmic Antibodies (Anca)

GMDN Terms

Code Name
55062 Multiple anti-neutrophil cytoplasmic antibody (ANCA) IVD, kit, enzyme immunoassay (EIA)

Identifiers

Type ID
Primary 04048474027778

Customer Contacts

Phone
973-564-7555

Premarket Submissions

Submission Number Supplement Number
K964448 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius