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Aquadex FlexFlow

FDA UDI

Class II (US FDA UDI)

by Gambro UF Solutions LLC

Identity

Trade Name
Aquadex FlexFlow FDA UDI
Generic Name
Haemofiltration system FDA UDI
Device Name
The Aquadex System is indicated for temporary (up to 8 hours) ultrafiltration treatment of patients with fluid overload who have failed diuretic therapy, and extended (longer than 8 hours) ultrafiltration treatment of patients with fluid overload who have failed diuretic therapy and require hospitalization. FDA UDI
Model / Reference
114158 FDA UDI
Description
The Aquadex System is indicated for temporary (up to 8 hours) ultrafiltration treatment of patients with fluid overload who have failed diuretic therapy, and extended (longer than 8 hours) ultrafiltration treatment of patients with fluid overload who have failed diuretic therapy and require hospitalization. FDA UDI

Identifiers

Catalog Number
114158 FDA UDI
Primary DI / UDI-DI
07332414112301 FDA UDI
FDA Product Code
KDI FDA UDI
GMDN Term
Haemofiltration system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5860 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Aquadex FlexFlow by Gambro UF Solutions LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f5228c4b-85a2-46bc-abfc-4cc9fd7c2797 37 fields · synced Jun 9, 2026