Duns Number:590153276
Device Description: Dryline Extension Kit
Catalog Number
RT024
Brand Name
Fisher & Paykel Healthcare
Version/Model Number
RT024
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
BZO
Product Code Name
Set, Tubing And Support, Ventilator (W Harness)
Public Device Record Key
93545ec1-6174-4805-8a3f-25a4125c6164
Public Version Date
August 10, 2022
Public Version Number
1
DI Record Publish Date
August 02, 2022
Package DI Number
09420012403353
Quantity per Package
20
Contains DI Package
09420012430625
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
PACK
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 159 |
2 | A medical device with a moderate to high risk that requires special controls. | 349 |