FDA UDI In Commercial Distribution 🇺🇸 United States

Coxiella burnetii (Q-Fever) Phase 1 IgG ELISA

DI: 00404847451887 · Model: EIA-5188 · 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 1 IgG ELISA
Primary DI
00404847451887
Version / Model
EIA-5188
Catalog Number
EIA-5188
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
1
Public Version Date
2021-06-15
Public Version Status
New
Public Device Record Key
6a782076-b615-4ea5-bd75-556cefe69b57

Device Description

The Coxiella burnetii (Q-Fever) Phase 1 IgG ELISA is intended for the qualitative determination of IgG class antibodies against Coxiella burnetii (Q-Fever) Phase 1 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 00404847451887

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius