FDA UDI In Commercial Distribution 🇺🇸 United States

Cytovale Reagent Kit

DI: 00860001900507 · Model: CV-REA-101 · Cytovale Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cytovale Reagent Kit
Primary DI
00860001900507
Version / Model
CV-REA-101
Catalog Number
CV-REA-101
Company Name
Cytovale Inc
Labeler DUNS
078418950
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-03
Public Version
1
Public Version Date
2025-07-11
Public Version Status
New
Public Device Record Key
64ee15ab-2242-4ec8-acde-0558b23bec18

Device Description

Cytovale Reagent Kit used to prepare the leukocyte suspension analyzed in the IntelliSep test by the Cytovale System. The two components in the Cytovale Reagent Kit: Reagent A (lysis solution w/ <1% formic acid) and Reagent B (quench w/ sodium carbonate).

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
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
QUT Deformability Cytometry For Sepsis Risk Assessment

GMDN Terms

Code Name
67567 Leukocyte deformability IVD, kit, rapid microfluidic cytometry

Identifiers

Type ID
Primary 00860001900507

Customer Contacts

Phone
415-417-2188

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
18 – 28 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
20 – 80 Percent (%) Relative Humidity