FDA UDI In Commercial Distribution 🇺🇸 United States

Coxiella burnetii (Q-Fever) Phase 2 IgG ELISA

DI: 04048474051896 · Model: EIA-5189 · DRG Instruments Gesellschaft mit beschränkter Haftung
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Coxiella burnetii (Q-Fever) Phase 2 IgG ELISA
Primary DI
04048474051896
Version / Model
EIA-5189
Catalog Number
EIA-5189
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
2023-09-01
Public Version
1
Public Version Date
2023-09-11
Public Version Status
New
Public Device Record Key
d784c603-603c-4ecc-9c5e-2b9b9da18bf8

Device Description

The Coxiella burnetii (Q-Fever) Phase 2 IgG ELISA is intended for the qualitative determination of IgG class antibodies against Coxiella burnetii (Q-Fever) Phase 2 in human serum or plasma (citrate, heparin).

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
GPR Antiserum, Cf, Q Fever

GMDN Terms

Code Name
51350 Coxiella burnetii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

Identifiers

Type ID
Primary 04048474051896

Customer Contacts

Phone
973-564-7555

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius