StarTrol

FDA UDI

Class II (US FDA UDI)

by Huot Instruments, Llc

Identity

Trade Name: StarTrol FDA UDI
Generic Name: Mobile examination/treatment room light FDA UDI
Device Name: Handel FDA UDI
Model / Reference: HND FDA UDI
Description: Handel FDA UDI

Identifiers

Catalog Number: HND FDA UDI
Primary DI / UDI-DI: M575HND0 FDA UDI
FDA Product Code: FSS FDA UDI
KZF FDA UDI
FTD FDA UDI
FSY FDA UDI
GMDN Term: Mobile examination/treatment room light FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4580 FDA UDI
880.6320 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

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Fixed examination/treatment room light Mobile examination/treatment room light

StarTrol by Huot Instruments, Llc — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Huot Instruments, Llc

Sources (1)

FDA UDI 3a0bccaa-1804-4b3c-a3c9-b0dda5aabf3e 35 fields · synced Jun 1, 2026