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Sentio

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
SENTIO FDA UDI
Generic Name
Analytical non-scalp cutaneous electrode FDA UDI
Device Name
SENTIO MMG SENSORS 8 PACK WITH GROUND FDA UDI
Model / Reference
286202108 FDA UDI
Description
SENTIO MMG SENSORS 8 PACK WITH GROUND FDA UDI

Identifiers

Catalog Number
286202108 FDA UDI
Primary DI / UDI-DI
20705034534753 FDA UDI
510(k) Number
K173526 FDA UDI
FDA Product Code
PDQ FDA UDI
ETN FDA UDI
GMDN Term
Analytical non-scalp cutaneous electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.1820 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Analytical non-scalp cutaneous electrode

Sentio by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analytical non-scalp cutaneous electrode.

Cleared under the same submission

K173526 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medos International Sàrl

Sources (1)

  • FDA UDI 0ca4fec8-7a90-49bf-95e9-b8e2d65bd2c9 36 fields · synced Jun 8, 2026