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ChoiceMMed MD300CL37

by Beijing Choice Electronic Technology Co., Ltd.

ChoiceMMed MD300CL37 is a Class II device made by Beijing Choice Electronic Technology Co., Ltd., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 06942820460265), 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 Number06942820460265 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
ChoiceMMed
Generic name
Pulse oximeter
Model / reference
MD300CL37
Primary DI / UDI-DI
06942820460265
FDA product code
DQA
GMDN term
Pulse oximeter
Device class
Class II
Regulation number
870.2700
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Pulse oximeter

Other devices from Beijing Choice Electronic Technology Co., Ltd.

See all devices from Beijing Choice Electronic Technology Co., Ltd. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)