gudid
Primary ID: Graft Slivering Board
Graft Slivering Board (UDI Graft Slivering Board)
Manufactured by Cole Instruments Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Graft Slivering Board - Primary ID Graft Slivering Board
Device Regulatory Overview
The Graft Slivering Board (Model/Catalog Number: Graft Slivering 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 Slivering Board
- Product Code / EMDN
- KET
- Device Name
- A dissection board used to dissect follicles from a strip of skin removed from the donor area of the scalp so that the follicles can be processed before it is transplanted into the recipient area. An LED backlight can be attached from 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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Graft Slivering Board?
The registered manufacturer of record for Graft Slivering Board is Cole Instruments Inc.
What is the Primary UDI-DI identifier for Graft Slivering Board?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Graft Slivering 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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