Duns Number:025460908
Device Description: TUBE,ET,REINFORCED CUFFED MURPHY 4MM
Catalog Number
DYNJAARC40
Brand Name
Medline Industries, Inc.
Version/Model Number
DYNJAARC40
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
K042683,K042683
Product Code
BTR
Product Code Name
Tube, tracheal (w/wo connector)
Public Device Record Key
a9b2c88d-ed80-4d5c-8f59-28568711c97d
Public Version Date
December 23, 2019
Public Version Number
3
DI Record Publish Date
October 15, 2015
Package DI Number
30080196504040
Quantity per Package
10
Contains DI Package
10080196504046
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 38540 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 85094 |
| 3 | A medical device with high risk that requires premarket approval | 2 |
| U | Unclassified | 7 |