Duns Number:078375583
Device Description: LED Surgical Light with center focus with optional camera capability
Catalog Number
-
Brand Name
Aurora Surgical Light Series
Version/Model Number
Aurora 3
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 19, 2016
Issuing Agency
In GS1
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FSS
Product Code Name
Light, surgical, floor standing
Public Device Record Key
173ac4ea-986b-462c-8511-03016ca7eb9a
Public Version Date
August 09, 2021
Public Version Number
5
DI Record Publish Date
September 19, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 747 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 265 |