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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
Ambulatory fall sensor FDA UDI
Device Name
Transmitter FDA UDI
Model / Reference
DTPC-TM FDA UDI
Description
Transmitter FDA UDI

Identifiers

Primary DI / UDI-DI
00812293016367 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Ambulatory fall 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

No

FDA UDI

Category: Ambulatory fall sensor

Smart Caregiver by Smart Caregiver Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ambulatory fall sensor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smart Caregiver Corporation

Sources (1)

  • FDA UDI 22eb0fef-2c3a-4eb7-a0c1-a7a4ed01fe2b 33 fields · synced May 30, 2026