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Parasol Wireless Patient Fall Prevention System

FDA UDI

Class I (US FDA UDI)

by Parasol Medical

Identity

Trade Name
Parasol Wireless Patient Fall Prevention System FDA UDI
Generic Name
Inpatient motion surveillance unit FDA UDI
Device Name
Wireless Falls Monitor ID Key FDA UDI
Model / Reference
KEY01 FDA UDI
Description
Wireless Falls Monitor ID Key FDA UDI

Identifiers

Primary DI / UDI-DI
00854636006642 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Inpatient motion surveillance unit 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

Category: Inpatient motion surveillance unit

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

Similar devices

Also classified as Inpatient motion surveillance unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Parasol Medical

Sources (1)

  • FDA UDI 9b0751dc-7b1f-4b75-b63d-fed931625adf 34 fields · synced May 30, 2026