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Matrix-2436ro, 5400gpd, 208v, 3mem

FDA UDI

Class II (US FDA UDI)

by Better Water, Inc.

Identity

Trade Name
MATRIX-2436RO, 5400GPD, 208V, 3MEM FDA UDI
Generic Name
Reverse-osmosis water purification system FDA UDI
Device Name
Reverse osmosis device for water purification for dialysis applications. Matrix 2436 series with digital HMI (touch-screen), three membranes, 208V. FDA UDI
Model / Reference
EQRMD-245K-3L FDA UDI
Description
Reverse osmosis device for water purification for dialysis applications. Matrix 2436 series with digital HMI (touch-screen), three membranes, 208V. FDA UDI

Identifiers

Catalog Number
EQRMD-245K-3L FDA UDI
Primary DI / UDI-DI
RO0404 FDA UDI
510(k) Number
K051620 FDA UDI
FDA Product Code
FIP FDA UDI
GMDN Term
Reverse-osmosis water purification system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5665 FDA UDI
Commercial Distribution
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

Category: Reverse-osmosis water purification system

Matrix-2436ro, 5400gpd, 208v, 3mem by Better Water, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Reverse-osmosis water purification system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Better Water, Inc.

Sources (1)

  • FDA UDI fa40a214-8859-4bbf-8240-01df9108f71d 35 fields · synced May 31, 2026