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Nexstim NBT software

FDA UDI

Class II (US FDA UDI)

by Nexstim Oyj

Identity

Trade Name
Nexstim NBT software FDA UDI
Generic Name
Stereotactic neuronavigation/planning system FDA UDI
Device Name
NBT main software FDA UDI
Model / Reference
2 FDA UDI
Description
NBT main software FDA UDI

Identifiers

Primary DI / UDI-DI
06430063200156 FDA UDI
FDA Product Code
GWF FDA UDI
IKN FDA UDI
HAW FDA UDI
OBP FDA UDI
GMDN Term
Stereotactic neuronavigation/planning system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1870 FDA UDI
890.1375 FDA UDI
882.4560 FDA UDI
882.5805 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

Yes

FDA UDI

Category: Stereotactic neuronavigation/planning system

Nexstim NBT software by Nexstim Oyj — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stereotactic neuronavigation/planning system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nexstim Oyj

Sources (1)

  • FDA UDI 09d2069d-b073-4e67-bf89-3859eaabc7a7 34 fields · synced May 30, 2026