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Care Mill

FDA UDI

Class II (US FDA UDI)

by Simpro

Identity

Trade Name
Care Mill FDA UDI
Generic Name
Automatic-inflation electronic sphygmomanometer, portable, finger FDA UDI
Device Name
Talking Upper Arm BP Monitor FDA UDI
Model / Reference
C01 FDA UDI
Description
Talking Upper Arm BP Monitor FDA UDI

Identifiers

Primary DI / UDI-DI
00810025923433 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Automatic-inflation electronic sphygmomanometer, portable, finger 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

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: Automatic-inflation electronic sphygmomanometer, portable, finger

Care Mill by Simpro — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Automatic-inflation electronic sphygmomanometer, portable, finger.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Simpro

Sources (1)

  • FDA UDI 071d7b5f-33e6-4811-9992-45ca3bcb6d69 33 fields · synced Jun 6, 2026