Skip to content

Dexcom Receiver MT22949

by Dexcom

Dexcom Receiver MT22949 is a Class III device made by Dexcom, listed in FDA GUDID since 10 Apr 2017 (UDI-DI 00386270000323), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00386270000323 UDI-DI Date10 Apr 2017ListedStatusListed GUDID: not 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  • Withdrawn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
Dexcom Receiver
Generic name
Percutaneous interstitial fluid glucose monitoring system, electrochemical
Model / reference
MT22949
Primary DI / UDI-DI
00386270000323
FDA product code
PQF
GMDN term
Percutaneous interstitial fluid glucose monitoring system, electrochemical
Device class
Class III
GUDID distribution status
Not in Commercial Distribution
MRI safety
MR Unsafe

Other devices from Dexcom

See all devices from Dexcom →

Properties

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