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HarmonyAIR

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name
HarmonyAIR FDA UDI
Generic Name
Medical monitor/light mount FDA UDI
Device Name
The A-Series High Definition Triple Light, No Drop Tube Adjustable is used with the HarmonyAIR A-Series Lighting System. FDA UDI
Model / Reference
A-Series Lighting System FDA UDI
Description
The A-Series High Definition Triple Light, No Drop Tube Adjustable is used with the HarmonyAIR A-Series Lighting System. FDA UDI

Identifiers

Catalog Number
LAH06INNDA FDA UDI
Primary DI / UDI-DI
00724995199647 FDA UDI
FDA Product Code
FSY FDA UDI
GMDN Term
Medical monitor/light mount FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4580 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Operating room light systemOperating room lightMedical monitor/light mount

HarmonyAIR by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical monitor/light mount.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 775716e3-f62b-4f2c-a6aa-28b8bf249ca6 35 fields · synced Jun 8, 2026