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Remote Monitoring

FDA UDI

Class II (US FDA UDI)

by Nuvasive, Inc.

Identity

Trade Name
Remote Monitoring FDA UDI
Generic Name
Neurophysiologic monitoring system FDA UDI
Device Name
NV RM Surface Module, NVM5 IOM MEP/EMG FDA UDI
Model / Reference
8025002 FDA UDI
Description
NV RM Surface Module, NVM5 IOM MEP/EMG FDA UDI

Identifiers

Primary DI / UDI-DI
00887517206688 FDA UDI
510(k) Number
K143641 FDA UDI
FDA Product Code
GWF FDA UDI
IKN FDA UDI
PDQ FDA UDI
HAW FDA UDI
OLO FDA UDI
ETN FDA UDI
GMDN Term
Neurophysiologic monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1870 FDA UDI
890.1375 FDA UDI
874.1820 FDA UDI
882.4560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Category: Neurophysiologic monitoring system

Remote Monitoring by Nuvasive, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurophysiologic monitoring system.

Cleared under the same submission

K143641 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nuvasive, Inc.

Sources (1)

  • FDA UDI 75465168-bc22-423e-ab8b-d6d0c20f9cc2 35 fields · synced Jun 7, 2026