FDA UDI Not in Commercial Distribution 🇺🇸 United States

frCRP

DI: 05055273201796 · Model: CP3850 · RANDOX LABORATORIES LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
frCRP
Primary DI
05055273201796
Version / Model
CP3850
Catalog Number
CP3850
Company Name
RANDOX LABORATORIES LIMITED
Labeler DUNS
227530649
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-09
Public Version
4
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
7acf2170-e577-4d17-aa84-5a9dc7c4171d
Distribution End Date
2016-09-16

Device Description

The CRP test system is intended for the quantitative in vitro determination of C-Reactive Protein (CRP) concentration in serum or plasma.

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DCK C-Reactive Protein, Antigen, Antiserum, And Control

GMDN Terms

Code Name
53707 C-reactive protein (CRP) IVD, reagent

Identifiers

Type ID
Primary 05055273201796

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K001009 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius