Duns Number:058614483
Device Description: Bronchoscope Adapter;For use with Olympus 190 bronchoscopes
Catalog Number
-
Brand Name
Edge
Version/Model Number
SD303BAPK
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"
Yes
For Single-Use
Yes
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
JAK
Product Code Name
System, x-ray, tomography, computed
Public Device Record Key
3ea62b95-aafe-49a0-b92f-a38cfe634ac9
Public Version Date
October 14, 2021
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
20884521539775
Quantity per Package
10
Contains DI Package
10884521539778
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 132 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 8540 |
| 3 | A medical device with high risk that requires premarket approval | 202 |
| U | Unclassified | 40 |