AmeriWater MRO6Z

FDA UDI

Class II (US FDA UDI)

by Ameriwater Llc.

Identity

Trade Name: AmeriWater MRO6Z FDA UDI
Generic Name: Reverse-osmosis water purification system FDA UDI
Device Name: MRO6Z 6 Membrane Reverse Osmosis System, up to 13,200 GPD, 208V, 230V, or 460V 3Ph FDA UDI
Model / Reference: MRO6Z FDA UDI
Description: MRO6Z 6 Membrane Reverse Osmosis System, up to 13,200 GPD, 208V, 230V, or 460V 3Ph FDA UDI

Identifiers

Primary DI / UDI-DI: 00817927020185 FDA UDI
510(k) Number: K131622 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Weight — 525 Pound FDA UDI
Width — 26 Inch FDA UDI
Height — 66 Inch FDA UDI
Depth — 46 Inch FDA UDI

Category: Reverse-osmosis water purification system

AmeriWater MRO6Z by Ameriwater Llc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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BioPure HX2 — Biolab Equipment Ltd · Class II

Cleared under the same submission

K131622 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Ameriwater Llc.

Sources (1)

FDA UDI 1a28ae2a-e14a-44ab-9d90-0972742ce7b9 35 fields · synced Jun 8, 2026