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23 G

FDA UDI

Class II (US FDA UDI)

by Mar Cor Purification, Inc.

Identity

Trade Name
23 G FDA UDI
Generic Name
Reverse-osmosis water purification system FDA UDI
Model / Reference
RO,23G-15K,208/230V,60HZ,75% FDA UDI

Identifiers

Primary DI / UDI-DI
00817492020269 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

Dimensions & Sizes

Size
Weight — 823 Pound FDA UDI
Height — 70 Inch FDA UDI
Depth — 82 Inch FDA UDI
Width — 29 Inch FDA UDI

Category: Reverse-osmosis water purification system

23 G by Mar Cor Purification, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Reverse-osmosis water purification system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eeb56ac8-3bc1-4a33-992a-e8a7436c0f0d 35 fields · synced May 30, 2026