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Dexcom G6 Receiver

FDA UDI

Class II (US FDA UDI)

by Dexcom

Identity

Trade Name
Dexcom G6 Receiver FDA UDI
Generic Name
Percutaneous interstitial fluid glucose monitoring system, electrochemical FDA UDI
Device Name
G6 Receiver FDA UDI
Model / Reference
MT24078 FDA UDI
Description
G6 Receiver FDA UDI

Identifiers

Primary DI / UDI-DI
00386270000583 FDA UDI
FDA Product Code
QBJ FDA UDI
GMDN Term
Percutaneous interstitial fluid glucose monitoring system, electrochemical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1355 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Percutaneous interstitial fluid glucose monitoring system, electrochemical

Dexcom G6 Receiver by Dexcom — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Percutaneous interstitial fluid glucose monitoring system, electrochemical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dexcom

Sources (1)

  • FDA UDI 4c15a78c-c87d-4361-8d63-5ded1cd4ae46 35 fields · synced Jun 1, 2026