FDA UDI In Commercial Distribution 🇺🇸 United States

AQUA

DI: 07340201503782 · Model: AQUA 3.3 · Elekta Solutions AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AQUA
Primary DI
07340201503782
Version / Model
AQUA 3.3
Company Name
Elekta Solutions AB
Labeler DUNS
353272181
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-10
Public Version
1
Public Version Date
2025-12-18
Public Version Status
New
Public Device Record Key
1ffe5e8a-f98f-4b42-80db-9894ce3a6643

Device Description

AQUA V3.3 Machine QA Software

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LHO Instrument, Quality-Assurance, Radiologic

GMDN Terms

Code Name
40887 Radiation therapy software

Identifiers

Type ID
Primary 07340201503782