FDA UDI In Commercial Distribution 🇺🇸 United States

SeroELISA Chlamydia IgG

DI: 07290001913147 · Model: A111-01 · SAVYON DIAGNOSTICS LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SeroELISA Chlamydia IgG
Primary DI
07290001913147
Version / Model
A111-01
Catalog Number
A111-01
Company Name
SAVYON DIAGNOSTICS LTD
Labeler DUNS
533708202
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-29
Public Version
1
Public Version Date
2025-06-06
Public Version Status
New
Public Device Record Key
00dd6e47-8247-4160-89fb-a6abb5f5fe6f

Device Description

The SeroELISA Chlamydia IgG kit is intended for the determination of specific IgG antibody to Chlamydia in a single human serum sample or to evaluate paired sera, by an Enzyme-Linked Immunosorbent Assay (ELISA).

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LJC Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group)

GMDN Terms

Code Name
50737 Chlamydia pneumoniae immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

Identifiers

Type ID
Primary 07290001913147

Premarket Submissions

Submission Number Supplement Number
K915281 000

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
2 – 8 Degrees Celsius