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Eversense E3 Pouch Containing Sensor and Holder

FDA UDI

Class III (US FDA UDI)

by Senseonics, Incorporated

Identity

Trade Name
Eversense E3 Pouch Containing Sensor and Holder FDA UDI
Generic Name
Implantable glucose monitoring system sensor FDA UDI
Device Name
Eversense E3 Pouch contains one Eversense E3 Sensor in a Sensor holder. FDA UDI
Model / Reference
102095-81A FDA UDI
Description
Eversense E3 Pouch contains one Eversense E3 Sensor in a Sensor holder. FDA UDI

Identifiers

Primary DI / UDI-DI
00817491023063 FDA UDI
PMA Number
P160048 FDA UDI
FDA Product Code
QHJ FDA UDI
GMDN Term
Implantable glucose monitoring system sensor FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
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 Conditional FDA UDI

Category: Implantable glucose monitoring system sensor

Eversense E3 Pouch Containing Sensor and Holder by Senseonics, Incorporated — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable glucose monitoring system sensor.

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 96aed5ad-1382-47d5-baad-c74093eac7cc 36 fields · synced Jun 7, 2026