FDA UDI In Commercial Distribution 🇺🇸 United States

Cytovale Reagent Kit

DI: 00860005204618 · Model: CV-REA-001 · Cytovale Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Cytovale Reagent Kit
Primary DI
00860005204618
Version / Model
CV-REA-001
Catalog Number
CV-REA-001
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
fee04016-f988-4b45-8586-0234c1cb821d

Device Description

Cytovale Reagent Kit used to prepare the leukocyte suspension for analysis 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 00860005204618
Package 00860005204670

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