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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 HarmonyAIR Hybrid Single Light, with Dual Flat Panel Monitor, 13-inch Drop Tube is a ceiling supported surgical lighting system of one or more E-Series lightheads. FDA UDI
Model / Reference
E-Series FDA UDI
Description
The HarmonyAIR Hybrid Single Light, with Dual Flat Panel Monitor, 13-inch Drop Tube is a ceiling supported surgical lighting system of one or more E-Series lightheads. FDA UDI

Identifiers

Catalog Number
LES56IN01 FDA UDI
Primary DI / UDI-DI
00724995175900 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
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 146039c0-c605-429a-b1bb-882671659763 36 fields · synced Jun 8, 2026