FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHO

DI: 10758750007523 · Model: 6902093 · ORTHO-CLINICAL DIAGNOSTICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ORTHO
Primary DI
10758750007523
Version / Model
6902093
Catalog Number
6902093
Company Name
ORTHO-CLINICAL DIAGNOSTICS, INC.
Labeler DUNS
068715424
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-24
Public Version
5
Public Version Date
2023-06-21
Public Version Status
Update
Public Device Record Key
41d21524-3f9e-4acc-83dd-edf0366e7d06

Device Description

Auto Reader IV

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MZA TEST,EQUIPMENT,AUTOMATED BLOODBORNE PATHOGEN

GMDN Terms

Code Name
57862 Microplate reader IVD, automated/semi-automated

Identifiers

Type ID
Primary 10758750007523

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 35 Degrees Celsius