Duns Number:008124539
Catalog Number
-
Brand Name
Resp-O2 Intubating Stylette, 12 FR
Version/Model Number
36267
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
Yes
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
BSR
Product Code Name
Stylet, Tracheal Tube
Public Device Record Key
dbb38d34-50b4-4bcd-9c3b-2a9e570b8e27
Public Version Date
May 25, 2022
Public Version Number
1
DI Record Publish Date
May 17, 2022
Package DI Number
00840117313439
Quantity per Package
10
Contains DI Package
00840117313422
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 | 694 |
2 | A medical device with a moderate to high risk that requires special controls. | 226 |
3 | A medical device with high risk that requires premarket approval | 2 |