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Wet-Stop

FDA UDI

Class II (US FDA UDI)

by Pottymd, Llc

Identity

Trade Name
Wet-Stop FDA UDI
Generic Name
Incontinence sensor/alarm FDA UDI
Device Name
Wet-Stop3 Enuresis Alarm FDA UDI
Model / Reference
WS103 FDA UDI
Description
Wet-Stop3 Enuresis Alarm FDA UDI

Identifiers

Primary DI / UDI-DI
00188813000247 FDA UDI
FDA Product Code
KPN FDA UDI
GMDN Term
Incontinence sensor/alarm FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.2040 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Incontinence sensor/alarm

Wet-Stop by Pottymd, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Incontinence sensor/alarm.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pottymd, Llc

Sources (1)

  • FDA UDI 88055dfc-cfd8-481a-a02f-1c9383a59617 33 fields · synced May 31, 2026