Duns Number:008124539
Device Description: Resp-O2 Heat Moisture Exchanger & B/V Filter (HMEF) 1000 CO2 Port, Low Profile, Adult
Catalog Number
-
Brand Name
Resp-O2 Heat Moisture Exchanger
Version/Model Number
30104
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K132709,K132709
Product Code
CAH
Product Code Name
Filter, Bacterial, Breathing-Circuit
Public Device Record Key
4c11eea0-a250-4e8b-b87b-1f4c0c2dbcd2
Public Version Date
January 31, 2022
Public Version Number
3
DI Record Publish Date
April 22, 2021
Package DI Number
00840117305328
Quantity per Package
50
Contains DI Package
00840117305311
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 |