FDA UDI In Commercial Distribution 🇺🇸 United States

HELIOS

DI: 04260186125096 · Model: AUTOMATED IFA SYSTEM · Aesku.Systems GmbH & Co. KG
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
HELIOS
Primary DI
04260186125096
Version / Model
AUTOMATED IFA SYSTEM
Catalog Number
IOS-1000
Company Name
Aesku.Systems GmbH & Co. KG
Labeler DUNS
341702675
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-02
Public Version
2
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
53c87a5d-6ffb-45c8-93f5-2517f770e335

Device Description

Automated system for immunofluorescence processing with an integral fluorescence microscope and software for routine laboratory use by professional users under controlled environmental conditions.

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
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
PIV Automated Indirect Immunofluorescence Microscope And Software-Assisted System For Clinical Use
DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control

GMDN Terms

Code Name
56705 Fluorescent immunoassay analyser IVD, laboratory

Identifiers

Type ID
Primary 04260186125096
Previous 42601861205090