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Graft Board Round LED Backlight

FDA UDI

Class I (US FDA UDI)

by Cole Instruments

Identity

Trade Name
Graft Board Round LED Backlight FDA UDI
Generic Name
Fibreoptic operating light system FDA UDI
Device Name
Round LED back light used for Graft Boards in processing FDA UDI
Model / Reference
Graft Board Round LED Backlight FDA UDI
Description
Round LED back light used for Graft Boards in processing FDA UDI

Identifiers

Catalog Number
614.000 FDA UDI
Primary DI / UDI-DI
00810072350947 FDA UDI
FDA Product Code
PEQ FDA UDI
GMDN Term
Fibreoptic operating light system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6320 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Fibreoptic operating light system

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

Similar devices

Also classified as Fibreoptic operating light system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cole Instruments

Sources (1)

  • FDA UDI 325bdfef-72bb-4bca-9d21-14d1972113e4 34 fields · synced Jun 1, 2026