Catalog Number

-

Brand Name

Dexcom Receiver

Version/Model Number

MT22949

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

P120005

Product Code

PQF

Product Code Name

Sensor, Glucose, Invasive, Non-Adjunctive

Public Device Record Key

096daf24-1b32-4de9-82d2-1e2392df0330

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

April 10, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-