FDA UDI In Commercial Distribution 🇺🇸 United States

EVOYA Platform

DI: 06438147366804 · Model: 5021-1000 · Wallac Oy
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EVOYA Platform
Primary DI
06438147366804
Version / Model
5021-1000
Catalog Number
5021-1000
Company Name
Wallac Oy
Labeler DUNS
540156544
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-29
Public Version
2
Public Version Date
2023-03-07
Public Version Status
Update
Public Device Record Key
33afc831-009f-4f54-8504-645a36b4e5da

Device Description

The Evoya Software Platform is an in vitro diagnostics modular software intended to be used together with Neonatal screening assay systems to enable workflow activities, data management, results analysis and reporting. The EVOYA Software Platform is intended to be used by trained laboratory professionals. The Evoya Software Platform is intended for in vitro diagnostic use.

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
Yes
Has Serial Number
No
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
JQP Calculator/Data Processing Module, For Clinical Use

GMDN Terms

Code Name
35477 Clinical laboratory information system

Identifiers

Type ID
Primary 06438147366804