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Pouch Containing Grafted Sensor and Holder, Eversense 365
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Pouch Containing Grafted Sensor and Holder, Eversense 365 FDA UDI
- Generic Name
- Implantable glucose monitoring system sensor FDA UDI
- Device Name
- Pouch contains one Eversense 365 Sensor in a Sensor holder. FDA UDI
- Model / Reference
- 102606-023 FDA UDI
- Description
- Pouch contains one Eversense 365 Sensor in a Sensor holder. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817491024220 FDA UDI
- 510(k) Number
- K241335 FDA UDI
- FDA Product Code
- SBA FDA UDI
- GMDN Term
- Implantable glucose monitoring system sensor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1357 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
MR Conditional FDA UDI
Category: Implantable glucose monitoring system sensor
Pouch Containing Grafted Sensor and Holder, Eversense 365 by Senseonics, Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Implantable glucose monitoring system sensor.
- Eversense E3 Sensor Kit - DME — SENSEONICS, INCORPORATED · Class III
- Eversense 365 Sensor Kit (Provider Purchase) — SENSEONICS, INCORPORATED · Class II
- Eversense E3 Sensor Kit - Retail — SENSEONICS, INCORPORATED · Class III
- Eversense 365 Sensor Kit (DME) — SENSEONICS, INCORPORATED · Class II
- Eversense 365 Sensor Kit (Retail) — SENSEONICS, INCORPORATED · Class II
- Eversense E3 Pouch Containing Sensor and Holder — SENSEONICS, INCORPORATED · Class III
- Eversense E3 Sensor Kit – Provider Purchase — SENSEONICS, INCORPORATED · Class III
Cleared under the same submission
K241335 also covers:
- Eversense 365 Adhesive Patches Kit — SENSEONICS, INCORPORATED
- Eversense 365 Mobile Application (Android) — SENSEONICS, INCORPORATED
- Eversense 365 Mobile Application (iOS) — SENSEONICS, INCORPORATED
- Eversense 365 Sensor Kit (DME) — SENSEONICS, INCORPORATED
- Eversense 365 Sensor Kit (Provider Purchase) — SENSEONICS, INCORPORATED
- Eversense 365 Sensor Kit (Retail) — SENSEONICS, INCORPORATED
- Eversense 365 Smart Transmitter Kit (DME) — SENSEONICS, INCORPORATED
- Eversense 365 Smart Transmitter Kit (Provider Purchase) — SENSEONICS, INCORPORATED
- Eversense 365 Smart Transmitter Kit (Retail) — SENSEONICS, INCORPORATED
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Senseonics, Incorporated
Sources (1)
- FDA UDI 3ed9a38e-e30a-44ab-8294-6b9382ce57f2 36 fields · synced Jun 8, 2026