Duns Number:506069240
Catalog Number
101135
Brand Name
MegaBeam® Reusable Fiber Optic Delivery System
Version/Model Number
MegaBeam® Reusable Bare Fiber 230um, Flat Tip, noID
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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
GEX
Product Code Name
Powered Laser Surgical Instrument
Public Device Record Key
ec0817e4-b2a0-4d10-844e-b9a0ef18caa8
Public Version Date
April 07, 2021
Public Version Number
4
DI Record Publish Date
January 31, 2017
Package DI Number
04049089300393
Quantity per Package
2
Contains DI Package
04049089200396
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 39 |