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Pro-Fit Eco-Flex

FDA UDI

Class I (US FDA UDI)

by Prime Pacific Health Innovations Corporation

Identity

Trade Name
Pro-Fit Eco-Flex FDA UDI
Generic Name
Colonic lavage kit, non-surgical FDA UDI
Device Name
The Pro-Fit Eco-Flex Regular Kit is a Colon Hydrotherapy Disposable Single-Use Speculum Kit consisting of a regular size speculum with insertion stop disc, a water inflow tube and a collapsible waste hose. FDA UDI
Model / Reference
Regular Kit with stop disc FDA UDI
Description
The Pro-Fit Eco-Flex Regular Kit is a Colon Hydrotherapy Disposable Single-Use Speculum Kit consisting of a regular size speculum with insertion stop disc, a water inflow tube and a collapsible waste hose. FDA UDI

Identifiers

Catalog Number
8116-EF FDA UDI
Primary DI / UDI-DI
07540198001067 FDA UDI
FDA Product Code
FFQ FDA UDI
GMDN Term
Colonic lavage kit, non-surgical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Colonic lavage kit, non-surgical

Pro-Fit Eco-Flex by Prime Pacific Health Innovations Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Colonic lavage kit, non-surgical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2f203f5f-5828-4a53-a786-3d74dab5d151 34 fields · synced Jun 6, 2026