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Care Mill C01

by Simpro

Care Mill C01 is a Class II device made by Simpro, listed in FDA GUDID since 2 Feb 2021 (UDI-DI 00810025923433), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810025923433 UDI-DI Date2 Feb 2021ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Care Mill
Generic name
Automatic-inflation electronic sphygmomanometer, portable, finger
Model / reference
C01
Primary DI / UDI-DI
00810025923433
FDA product code
DXN
GMDN term
Automatic-inflation electronic sphygmomanometer, portable, finger
Device class
Class II
Regulation number
870.1130
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code DXN (System, Measurement, Blood-Pressure, Non-Invasive).

Other devices from Simpro

See all devices from Simpro →

Properties

  • Over-the-counter
  • Premarket exempt
Other properties (13, all answered No)