FDA UDI In Commercial Distribution 🇺🇸 United States

iQ200

DI: 10837461001300 · Model: Select Plus Kit 2008 Analyzer (NA)/ Select Pro (NA) · BECKMAN COULTER IRELAND INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iQ200
Primary DI
10837461001300
Version / Model
Select Plus Kit 2008 Analyzer (NA)/ Select Pro (NA)
Catalog Number
700-3345
Company Name
BECKMAN COULTER IRELAND INC.
Labeler DUNS
985071975
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-07
Public Version
5
Public Version Date
2023-10-13
Public Version Status
Update
Public Device Record Key
dee5faf1-8cd0-4626-9ed4-b6003078018c

Device Description

"iQ200 Select 2008 Tested;800-3935 iQ®200 Select Plus Kit 2008 Analyzer (NA) "iQ200 Select 2008 Tested; 800-3051 iQ®200 Select Pro (NA); 800-3050 IRICELL 1000 Pro (NA); 800-3048 IRICELL 3000 Pro (NA)"

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KQO Automated Urinalysis System
LKM Counter, Urine Particle

GMDN Terms

Code Name
35918 Urine analyser IVD, laboratory

Identifiers

Type ID
Primary 10837461001300

Premarket Submissions

Submission Number Supplement Number
K022774 000