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Trackstar

FDA UDI

Class II (US FDA UDI)

by Veridian Healthcare

Identity

Trade Name
Trackstar FDA UDI
Generic Name
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI
Device Name
TRACKSTAR DIGITAL ARM BP MONITOR, BLUETOOTH FDA UDI
Model / Reference
302-2110B FDA UDI
Description
TRACKSTAR DIGITAL ARM BP MONITOR, BLUETOOTH FDA UDI

Identifiers

Primary DI / UDI-DI
00845717012096 FDA UDI
510(k) Number
K241351 FDA UDI
FDA Product Code
DXQ FDA UDI
GMDN Term
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1120 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

Trackstar by Veridian Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Automatic-inflation electronic sphygmomanometer, portable, arm/wrist.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Veridian Healthcare

Sources (1)

  • FDA UDI 81da0f86-a718-478c-be0b-01158ed3cc4c 34 fields · synced May 29, 2026