FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHO

DI: 10758750005260 · Model: 930740 · ORTHO-CLINICAL DIAGNOSTICS, INC.
Product Codes
0
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ORTHO
Primary DI
10758750005260
Version / Model
930740
Catalog Number
930740
Company Name
ORTHO-CLINICAL DIAGNOSTICS, INC.
Labeler DUNS
068715424
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-10-22
Public Version
7
Public Version Date
2023-04-14
Public Version Status
Update
Public Device Record Key
0e31108b-df6e-4fc9-b334-17a7a2e651a8

Device Description

ORTHO® HCV Version 3.0 ELISA Test System

Device Characteristics

Single Use
No
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
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

GMDN Terms

Code Name
48381 Hepatitis C virus antibody/antigen IVD, kit, enzyme immunoassay (EIA)

Identifiers

Type ID
Primary 10758750005260

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius