Duns Number:058614483
Device Description: Pediatric Tracheostomy Tube Long Cuffless
Catalog Number
-
Brand Name
Shiley
Version/Model Number
5.0PELF
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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
K122531,K182861,K122531,K182861
Product Code
JOH
Product Code Name
Tube tracheostomy and tube cuff
Public Device Record Key
87c8c50c-7439-45dc-ad1b-9dc8fc4e0bc2
Public Version Date
April 19, 2022
Public Version Number
4
DI Record Publish Date
May 04, 2019
Package DI Number
10884521779877
Quantity per Package
48
Contains DI Package
20884521779874
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 |