FDA UDI In Commercial Distribution 🇺🇸 United States

New Life Diagnostics

DI: 00850078606372 · Model: Ancylostoma IgG ELISA Kit · NEW LIFE DIAGNOSTICS LLC
Product Codes
0
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
New Life Diagnostics
Primary DI
00850078606372
Version / Model
Ancylostoma IgG ELISA Kit
Catalog Number
5041
Company Name
NEW LIFE DIAGNOSTICS LLC
Labeler DUNS
081986839
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-16
Public Version
1
Public Version Date
2026-04-24
Public Version Status
New
Public Device Record Key
b4221070-3cac-497a-8b47-1a38ad626d86

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
Yes
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

GMDN Terms

Code Name
64705 Assay development analyte-specific reagent IVD

Identifiers

Type ID
Primary 00850078606372