← Back to catalogue

Sentio

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
SENTIO FDA UDI
Generic Name
Nerve-function monitor FDA UDI
Device Name
SENTIO MMG TABLET WITH SENTIO MMG SW FDA UDI
Model / Reference
286202300 FDA UDI
Description
SENTIO MMG TABLET WITH SENTIO MMG SW FDA UDI

Identifiers

Catalog Number
286202300 FDA UDI
Primary DI / UDI-DI
10705034534787 FDA UDI
510(k) Number
K173526 FDA UDI
FDA Product Code
ETN FDA UDI
PDQ FDA UDI
GMDN Term
Nerve-function monitor 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nerve-function monitor

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

Similar devices

Also classified as Nerve-function monitor.

Cleared under the same submission

K173526 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medos International Sàrl

Sources (1)

  • FDA UDI 189c7164-b08e-40df-9b12-9400fa669f06 36 fields · synced May 30, 2026