FDA UDI In Commercial Distribution 🇺🇸 United States

AquaFlexFlow UF 500

DI: 10853072007128 · Model: 114157 · Nuwellis Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
AquaFlexFlow UF 500
Primary DI
10853072007128
Version / Model
114157
Catalog Number
114157
Company Name
Nuwellis Inc.
Labeler DUNS
790580182
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-03
Public Version
4
Public Version Date
2026-03-16
Public Version Status
Update
Public Device Record Key
3a818698-e11b-4583-8cf5-b7740c515f7c

Device Description

For use with the Aquadex System. The Aquadex System is indicated for: Continuous ultrafiltration therapy for temporary (up to 8 hours) or extended (longer than 8 hours in patients who require hospitalization) use in adult and pediatric patients weighing 20 kilograms or more whose fluid overload is unresponsive to medical management, including diuretics. All treatments must be administered within an outpatient or inpatient clinical setting by a healthcare provider, under physician prescription, both of whom having received training in extracorporeal therapies.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

GMDN Terms

Code Name
44601 Haemofilter

Identifiers

Type ID
Primary 10853072007128
Package 30853072007146

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K192756 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius