← Back to catalogue

Aquanet

FDA UDI

Class II (US FDA UDI)

by Prime Pacific Health Innovations Corporation

Identity

Trade Name
Aquanet FDA UDI
Generic Name
Colonic lavage unit FDA UDI
Device Name
The Aquanet EC-2000 is a colon hydrotherapy device. It introduces water at a comfortable temperature into the large intestine. It is a system for filling and emptying water into and out of the colon and thus cleansing the colon of its contents when medically indicated such as before radiological or endoscopic examination. FDA UDI
Model / Reference
EC-2000 FDA UDI
Description
The Aquanet EC-2000 is a colon hydrotherapy device. It introduces water at a comfortable temperature into the large intestine. It is a system for filling and emptying water into and out of the colon and thus cleansing the colon of its contents when medically indicated such as before radiological or endoscopic examination. FDA UDI

Identifiers

Catalog Number
4310 FDA UDI
Primary DI / UDI-DI
07540198000114 FDA UDI
510(k) Number
K000031 FDA UDI
FDA Product Code
KPL FDA UDI
GMDN Term
Colonic lavage unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5220 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: Colonic lavage unit

Aquanet by Prime Pacific Health Innovations Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Colonic lavage unit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 14c39988-f4df-4564-bf75-8f67ae93592e 35 fields · synced May 30, 2026