← Back to catalogue

Veridian Healthcare

FDA UDI

Class II (US FDA UDI)

by Veridian Healthcare

Identity

Trade Name
Veridian Healthcare FDA UDI
Generic Name
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI
Device Name
SmartHeart Wrist Blood Pressure Monitor FDA UDI
Model / Reference
01-574 FDA UDI
Description
SmartHeart Wrist Blood Pressure Monitor FDA UDI

Identifiers

Primary DI / UDI-DI
00845717011020 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1130 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Veridian Healthcare 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Veridian Healthcare

Sources (1)

  • FDA UDI 72ac239f-ed99-4726-839c-512dd0858142 34 fields · synced Jun 1, 2026