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Smart Caregiver

FDA UDI

Class I (US FDA UDI)

by Smart Caregiver Corporation

Identity

Trade Name
Smart Caregiver FDA UDI
Generic Name
Inpatient motion surveillance unit FDA UDI
Device Name
Retail Packaged Motion Sensor Alarm FDA UDI
Model / Reference
RP-TL-2700 FDA UDI
Description
Retail Packaged Motion Sensor Alarm FDA UDI

Identifiers

Primary DI / UDI-DI
00812293015841 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

No

FDA UDI

Category: Inpatient motion surveillance unit

Smart Caregiver by Smart Caregiver Corporation — 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

Sources (1)

  • FDA UDI 1de06e54-74fb-4507-8619-0f92efc7a92b 33 fields · synced Jun 8, 2026