FDA UDI In Commercial Distribution 🇺🇸 United States

Bordetella pertussis IgG ELISA

DI: 00404847434507 · Model: EIA-3450 · DRG Instruments Gesellschaft mit beschränkter Haftung
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bordetella pertussis IgG ELISA
Primary DI
00404847434507
Version / Model
EIA-3450
Catalog Number
EIA-3450
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
2021-06-07
Public Version
2
Public Version Date
2021-08-09
Public Version Status
Update
Public Device Record Key
03f757a4-a42a-4882-b2c5-147531ba8371

Device Description

The DRG Bordetella pertussis IgG Enzyme Immunoassay Kit provides materials for the qualitative and semi-quantitative determination of IgG-class antibodies to Bordetella pertussis and Bordetella pertussis toxin in serum and plasma (EDTA-, heparin- or citrate plasma). This assay is intended for in vitro diagnostic use only.

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
Yes
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
GOX ANTIGEN, B. PERTUSSIS

GMDN Terms

Code Name
50529 Bordetella pertussis immunoglobulin A (IgA)/IgG/IgM antibody IVD, kit, enzyme immunoassay (EIA)

Identifiers

Type ID
Primary 00404847434507

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius