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Eversense® Sensor Kit

FDA UDI

Class III (US FDA UDI)

by Senseonics, Incorporated

Identity

Trade Name
Eversense® Sensor Kit FDA UDI
Generic Name
Implantable glucose monitoring system sensor FDA UDI
Device Name
Eversense Sensor Kit contains one Eversense Sensor. FDA UDI
Model / Reference
FG-4200-00-301 FDA UDI
Description
Eversense Sensor Kit contains one Eversense Sensor. FDA UDI

Identifiers

Catalog Number
FG-4200-00-301 FDA UDI
Primary DI / UDI-DI
00817491021410 FDA UDI
PMA Number
P160048 FDA UDI
FDA Product Code
QCD FDA UDI
GMDN Term
Implantable glucose monitoring system sensor FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Eversense® Sensor Kit by Senseonics, Incorporated — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 d79e8dee-dd3a-4c0a-a4a6-86548ad2f908 38 fields · synced Jun 1, 2026