gudid Primary ID: Graft Processing Board

Graft Processing Board (UDI Graft Processing Board)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Graft Processing Board (Model/Catalog Number: Graft Processing Board) is a medical device manufactured by Cole Instruments Inc. This product is indexed under FDA Product Code / Category Classification KET within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Graft Processing Board
Product Code / EMDN: KET
Device Name: This is a dissecting board used to cut skin away from follicles after the follicles have been extracted from the donor area. A round LED backlight can be attached underneath to aid in this dissection.
Database Sync Date: 2026-08-09 09:09:55

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Graft Processing Board?

The registered manufacturer of record for Graft Processing Board is Cole Instruments Inc.

What is the Primary UDI-DI identifier for Graft Processing Board?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Graft Processing Board.

What classification code is assigned to this device?

This device is registered under product classification code KET.

Similar Classification Devices (KET)

Other Devices by Cole Instruments Inc

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