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Procare Basic Upper Arm BP Monitor

FDA UDI

Class II (US FDA UDI)

by Arise Medical Llc

Identity

Trade Name
Procare Basic Upper Arm BP Monitor FDA UDI
Generic Name
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI
Device Name
Upparm Arm blood pressure monitor with standard cuff FDA UDI
Model / Reference
240484 FDA UDI
Description
Upparm Arm blood pressure monitor with standard cuff FDA UDI

Identifiers

Primary DI / UDI-DI
00372217004035 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

Procare Basic Upper Arm BP Monitor by Arise Medical Llc — 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

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Manufacturer

Manufacturer
Arise Medical Llc

Sources (1)

  • FDA UDI 6123a13d-8795-4daf-9439-f1735250b18c 33 fields · synced May 30, 2026