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MediMax Tech

FDA UDI

Class II (US FDA UDI)

by Medimax Tech Inc.

Identity

Trade Name
MediMax Tech FDA UDI
Generic Name
Neuromuscular transmission motion sensor FDA UDI
Device Name
MF2409: Ring, Surface EMG Electrodes, Pet Film, 8x107mm, Hydrogel FDA UDI
Model / Reference
MF2409 Surface Electrodes FDA UDI
Description
MF2409: Ring, Surface EMG Electrodes, Pet Film, 8x107mm, Hydrogel FDA UDI

Identifiers

Primary DI / UDI-DI
00817325020398 FDA UDI
510(k) Number
K153019 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Neuromuscular transmission motion sensor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1320 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Neuromuscular transmission motion sensor

MediMax Tech by Medimax Tech Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neuromuscular transmission motion sensor.

Cleared under the same submission

K153019 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medimax Tech Inc.

Sources (1)

  • FDA UDI 5868710f-16ed-4443-9190-c1116950d095 35 fields · synced Jun 6, 2026