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neuro|mate® - Tool-holder locking screw

FDA UDI

Class II (US FDA UDI)

by Renishaw Mayfield

Identity

Trade Name
neuro|mate® - Tool-holder locking screw FDA UDI
Generic Name
Neurological stereotactic surgery system FDA UDI
Device Name
Tightening screw used to lock the tool adaptor into the neuro|mate tool-holder. FDA UDI
Model / Reference
Screw FDA UDI
Description
Tightening screw used to lock the tool adaptor into the neuro|mate tool-holder. FDA UDI

Identifiers

Catalog Number
005.0744 FDA UDI
Primary DI / UDI-DI
03662724000062 FDA UDI
510(k) Number
K132755 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Neurological stereotactic surgery system

neuro|mate® - Tool-holder locking screw by Renishaw Mayfield — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurological stereotactic surgery system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Renishaw Mayfield

Sources (1)

  • FDA UDI ef18c953-c9a4-465e-a8e2-e1b0bf9f8a03 36 fields · synced Jun 8, 2026