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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
Patient identification band FDA UDI
Device Name
Wristband Tester FDA UDI
Model / Reference
TL-4005DT FDA UDI
Description
Wristband Tester FDA UDI

Identifiers

Primary DI / UDI-DI
00812293016459 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Patient identification band 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: Patient identification band

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

Similar devices

Also classified as Patient identification band.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1b1e09ab-b17b-4812-82ec-a32d3b56d69e 33 fields · synced Jun 6, 2026