FDA UDI In Commercial Distribution 🇺🇸 United States

Alere Rubella-plus®

DI: 10859035006245 · Model: 84R2 · ALERE NORTH AMERICA, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
30

Basic Information

Brand Name
Alere Rubella-plus®
Primary DI
10859035006245
Version / Model
84R2
Company Name
ALERE NORTH AMERICA, LLC
Labeler DUNS
826027364
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
b2ea90a8-a0b9-47a9-a33f-4ea75f9d9b25

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LFX Enzyme Linked Immunoabsorbent Assay, Rubella

GMDN Terms

Code Name
50265 Rubella virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

Identifiers

Type ID
Primary 10859035006245
Unit of Use 00859035006248

Customer Contacts

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
2 – 8 Degrees Celsius