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Parasol Patient Fall Prevention System

FDA UDI

Class I (US FDA UDI)

by Parasol Medical

Identity

Trade Name
Parasol Patient Fall Prevention System FDA UDI
Generic Name
Bed/chair occupant movement pressure/vibration sensor FDA UDI
Device Name
30 Day Potty Pad with 3 Foot Cord FDA UDI
Model / Reference
SP6S3 FDA UDI
Description
30 Day Potty Pad with 3 Foot Cord FDA UDI

Identifiers

Primary DI / UDI-DI
00854636006338 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Bed/chair occupant movement pressure/vibration sensor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2400 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 5 Inch FDA UDI
Width — 2.5 Inch FDA UDI

Category: Bed/chair occupant movement pressure/vibration sensor

Parasol Patient Fall Prevention System by Parasol Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bed/chair occupant movement pressure/vibration sensor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Parasol Medical

Sources (1)

  • FDA UDI 0a4343da-d5b4-4436-8005-7058010ed622 34 fields · synced May 30, 2026