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Neuromate Planning Station Hardware

FDA UDI

Class II (US FDA UDI)

by Renishaw Mayfield

Identity

Trade Name
Neuromate Planning Station Hardware FDA UDI
Generic Name
Neurological stereotactic surgery system FDA UDI
Model / Reference
neuroinspire PC - Laptop US FDA UDI

Identifiers

Catalog Number
001.0130 FDA UDI
Primary DI / UDI-DI
03662724000451 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Neurological stereotactic surgery system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Neurological stereotactic surgery system

Neuromate Planning Station Hardware by Renishaw Mayfield — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurological stereotactic surgery system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Renishaw Mayfield

Sources (1)

  • FDA UDI 8fdc30b2-96db-4d90-91f3-f3b189717487 33 fields · synced May 30, 2026