FDA UDI In Commercial Distribution 🇺🇸 United States

Hemochron Whole Blood Coagulation System

DI: 10711234520048 · Model: HRS.RF · ACCRIVA DIAGNOSTICS HOLDINGS, INC.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Hemochron Whole Blood Coagulation System
Primary DI
10711234520048
Version / Model
HRS.RF
Catalog Number
HRS.RF
Company Name
ACCRIVA DIAGNOSTICS HOLDINGS, INC.
Labeler DUNS
079299318
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
6
Public Version Date
2022-12-22
Public Version Status
Update
Public Device Record Key
e3236dbc-1e87-4574-a9f1-c5bb0a630528

Device Description

Hemochron Whole Blood Coagulation System - Hemochron Response Instrument Refurbished

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
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
JPA System, Multipurpose For In Vitro Coagulation Studies

GMDN Terms

Code Name
62540 Coagulation analyser IVD, point-of-care, line-powered
56689 Coagulation analyser IVD, laboratory

Identifiers

Type ID
Primary 10711234520048

Customer Contacts