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Eversense Power Adapter

FDA UDI

Class III (US FDA UDI)

by Senseonics, Incorporated

Identity

Trade Name
Eversense Power Adapter FDA UDI
Generic Name
Implantable glucose monitoring system transmitter FDA UDI
Device Name
Power Adapter (i.e., wall plug) FDA UDI
Model / Reference
FG-6000-01-303 FDA UDI
Description
Power Adapter (i.e., wall plug) FDA UDI

Identifiers

Catalog Number
N/A FDA UDI
Primary DI / UDI-DI
00817491023858 FDA UDI
PMA Number
P160048 FDA UDI
FDA Product Code
QHJ FDA UDI
GMDN Term
Implantable glucose monitoring system transmitter FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Implantable glucose monitoring system transmitter

Eversense Power Adapter by Senseonics, Incorporated — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable glucose monitoring system transmitter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c5383124-f3ce-413b-a9e3-d3fc9f8e4524 36 fields · synced Jun 8, 2026