FDA UDI In Commercial Distribution 🇺🇸 United States

AU

DI: 15099590010966 · Model: OSR61105 · Beckman Coulter, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AU
Primary DI
15099590010966
Version / Model
OSR61105
Company Name
Beckman Coulter, Inc.
Labeler DUNS
008254708
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
3ae043c8-344c-4748-aeeb-02c1ea9ac218

Device Description

RF Latex

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
No
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

Product Codes

Code Name
DHR System, Test, Rheumatoid Factor

GMDN Terms

Code Name
55111 Rheumatoid factor IVD, kit, nephelometry/turbidimetry

Identifiers

Type ID
Primary 15099590010966

Premarket Submissions

Submission Number Supplement Number
K060201 000