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neuro|mate® - Frameless Head-holder - Clip

FDA UDI

Class II (US FDA UDI)

by Renishaw Mayfield

Identity

Trade Name
neuro|mate® - Frameless Head-holder - Clip FDA UDI
Generic Name
Neurological stereotactic surgery system FDA UDI
Device Name
A part of the Frameless Head-holder kit, the clip fixes the Head-holder ring onto the head-holder attachment. FDA UDI
Model / Reference
Frameles head-holder kit FDA UDI
Description
A part of the Frameless Head-holder kit, the clip fixes the Head-holder ring onto the head-holder attachment. FDA UDI

Identifiers

Catalog Number
004.0019 FDA UDI
Primary DI / UDI-DI
03662724000239 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
Not 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

neuro|mate® - Frameless Head-holder - Clip by Renishaw Mayfield — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Renishaw Mayfield

Sources (1)

  • FDA UDI f44f5bd0-2d72-4be1-9014-ed81774c4703 36 fields · synced Jun 8, 2026