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Pathway

FDA UDI

Class II (US FDA UDI)

by Prometheus Group Of New Hampshire Limited, The

Identity

Trade Name
Pathway FDA UDI
Generic Name
Psychophysiological biofeedback system FDA UDI
Device Name
Pathway® CTS 1500 FDA UDI
Model / Reference
CTS1500 FDA UDI
Description
Pathway® CTS 1500 FDA UDI

Identifiers

Catalog Number
CTS1500 FDA UDI
Primary DI / UDI-DI
00852423006028 FDA UDI
FDA Product Code
KPI FDA UDI
GMDN Term
Psychophysiological biofeedback system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5320 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Psychophysiological biofeedback systemPerineal orifice incontinence-control electrical stimulation system, professional

Pathway by Prometheus Group Of New Hampshire Limited, The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Perineal orifice incontinence-control electrical stimulation system, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3c6f9acd-cd37-4ac8-872b-81cb5afdca10 35 fields · synced May 30, 2026