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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
Perineometer FDA UDI
Device Name
Pathway® MR-25 Dual Channel EMG FDA UDI
Model / Reference
MR-25 FDA UDI
Description
Pathway® MR-25 Dual Channel EMG FDA UDI

Identifiers

Catalog Number
9725 FDA UDI
Primary DI / UDI-DI
00852423006042 FDA UDI
FDA Product Code
HIR FDA UDI
GMDN Term
Perineometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1425 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

Yes

FDA UDI

Category: Psychophysiological biofeedback systemPerineometer

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 Perineometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8a641225-6a7f-4029-90a9-db027402bf0d 35 fields · synced Jun 8, 2026