Duns Number:092673953
Device Description: Anesthesia Circuit, adult, 96" expandable parallel WYE w/GSP, GSE, In-Line HMEF, 3L not ma Anesthesia Circuit, adult, 96" expandable parallel WYE w/GSP, GSE, In-Line HMEF, 3L not made with latex breathing bag, GSL, 10' x .50 ID M/F, B/V Filter
Catalog Number
-
Brand Name
Disposable Anesthesia Circuits
Version/Model Number
9344
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
K922492,K922492
Product Code
CAH
Product Code Name
Filter, Bacterial, Breathing-Circuit
Public Device Record Key
d8a945f7-efb8-4c52-b7d6-4eba626eee0a
Public Version Date
October 24, 2022
Public Version Number
2
DI Record Publish Date
September 30, 2020
Package DI Number
10709078011211
Quantity per Package
20
Contains DI Package
00709078011214
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 | 746 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 320 |