Graft Processing Board

FDA UDI

Class I (US FDA UDI)

by Cole Instruments

Identity

Trade Name: Graft Processing Board FDA UDI
Generic Name: Surgical cutting/shaping board, reusable FDA UDI
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. FDA UDI
Model / Reference: Graft Processing Board FDA UDI
Description: 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. FDA UDI

Identifiers

Catalog Number: 601.000 FDA UDI
Primary DI / UDI-DI: 00810072351180 FDA UDI
FDA Product Code: KET FDA UDI
GMDN Term: Surgical cutting/shaping board, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 864.3010 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical cutting/shaping board, reusable

Graft Processing Board by Cole Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Cole Instruments

Sources (1)

FDA UDI 7307c03e-29fa-4f60-8060-0e4b861a5ae4 34 fields · synced Jun 8, 2026