Duns Number:066087031
Device Description: Oropharyngeal Airway, Size 120 mm, Non-Sterile
Catalog Number
OA122
Brand Name
Endure
Version/Model Number
OA1221217
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
CAE
Product Code Name
Airway, Oropharyngeal, Anesthesiology
Public Device Record Key
983fc2c8-7bc1-43eb-8d5c-90a6ab936881
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
February 20, 2018
Package DI Number
B531OA1222
Quantity per Package
10
Contains DI Package
B531OA1221
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Carton
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 40 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 36 |