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MyndMove

FDA UDI

Class II (US FDA UDI)

by Myndtec, Inc.

Identity

Trade Name
MyndMove FDA UDI
Generic Name
Neuromuscular transmission electrode FDA UDI
Model / Reference
MyndMove Electrode 2.5 D FDA UDI

Identifiers

Catalog Number
900168 FDA UDI
Primary DI / UDI-DI
00692520001683 FDA UDI
510(k) Number
K170564 FDA UDI
FDA Product Code
IPF FDA UDI
GZI FDA UDI
GMDN Term
Neuromuscular transmission electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5850 FDA UDI
882.5810 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Neuromuscular transmission electrode

MyndMove by Myndtec, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neuromuscular transmission electrode.

Cleared under the same submission

K170564 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Myndtec, Inc.

Sources (1)

  • FDA UDI 78228719-6986-4f8b-a662-4f9440e42d02 34 fields · synced May 30, 2026