FDA UDI In Commercial Distribution 🇺🇸 United States

HELIOS® AUTOMATED IFA SYSTEM

DI: 04250289512541 · Model: REF.IOS-1000 · Aesku.Diagnostics GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HELIOS® AUTOMATED IFA SYSTEM
Primary DI
04250289512541
Version / Model
REF.IOS-1000
Catalog Number
REF.IOS-1000
Company Name
Aesku.Diagnostics GmbH & Co. KG
Labeler DUNS
341714388
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-25
Public Version
1
Public Version Date
2023-07-03
Public Version Status
New
Public Device Record Key
57490d14-54b3-4938-839a-cc80632096f9

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
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

GMDN Terms

Code Name
56705 Fluorescent immunoassay analyser IVD, laboratory

Identifiers

Type ID
Primary 04250289512541

Premarket Submissions

Submission Number Supplement Number
K153117 000