FDA UDI In Commercial Distribution 🇺🇸 United States

ACCUTEST H. Pylori Rapid Test Device (Whole Blood/Serum) *CLIA-Waived*

DI: 10763924392206 · Model: ID392 · JANT PHARMACAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
ACCUTEST H. Pylori Rapid Test Device (Whole Blood/Serum) *CLIA-Waived*
Primary DI
10763924392206
Version / Model
ID392
Company Name
JANT PHARMACAL CORPORATION
Labeler DUNS
797393659
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2016-09-20
Public Version
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
09347972-ec7c-4b55-826d-166fbae0ab39

Device Description

ACCUTEST H. Pylori Rapid Test Device (Whole Blood/Serum) *CLIA-Waived*

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LYR Helicobacter Pylori

GMDN Terms

Code Name
30825 Helicobacter pylori antigen IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Primary 10763924392206
Unit of Use 00726924392204