HarmonyAIR - The HarmonyAIR G-Series Single Light, Non-Camera, - STERIS CORPORATION

Duns Number:036985604

Device Description: The HarmonyAIR G-Series Single Light, Non-Camera, Tandem G2 is used with the HarmonyAIR G- The HarmonyAIR G-Series Single Light, Non-Camera, Tandem G2 is used with the HarmonyAIR G-Series Lighting System.

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More Product Details

Catalog Number

LG01VNT

Brand Name

HarmonyAIR

Version/Model Number

G-Series Lighting System

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

FSY

Product Code Name

Light, surgical, ceiling mounted

Device Record Status

Public Device Record Key

e2e83a4a-884c-4478-a185-77f4081c5954

Public Version Date

August 13, 2021

Public Version Number

1

DI Record Publish Date

August 05, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"STERIS CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1528
2 A medical device with a moderate to high risk that requires special controls. 1557