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3CPM Company, Inc.

FDA UDI

Class II (US FDA UDI)

by 3CPM Company, Inc.

Identity

Trade Name
3CPM Company, Inc. FDA UDI
Generic Name
Myoelectric gastrointestinal motility analysis system FDA UDI
Device Name
3CPM EGGSAS Research/Waterload Interface (Software Only) FDA UDI
Model / Reference
2.09g FDA UDI
Description
3CPM EGGSAS Research/Waterload Interface (Software Only) FDA UDI

Identifiers

Primary DI / UDI-DI
00864359000292 FDA UDI
FDA Product Code
MYE FDA UDI
GMDN Term
Myoelectric gastrointestinal motility analysis system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1735 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Myoelectric gastrointestinal motility analysis system

3CPM Company, Inc. by 3CPM Company, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Myoelectric gastrointestinal motility analysis system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3CPM Company, Inc.

Sources (1)

  • FDA UDI e7d8c114-4edf-4ee4-a93b-54ed32f4cf04 33 fields · synced May 30, 2026