Duns Number:003080678
Device Description: Hopkins 'The Wave' Pulse Ox-Cobalt
Catalog Number
594029-159
Brand Name
Hopkins Medical Products®
Version/Model Number
594029-159
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"
-
For Single-Use
-
Prescription Use (Rx)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
DQA
Product Code Name
Oximeter
Public Device Record Key
0b78a543-56a2-48cb-84bd-2fecd2bfbf0c
Public Version Date
November 10, 2021
Public Version Number
2
DI Record Publish Date
September 28, 2018
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 96 |
2 | A medical device with a moderate to high risk that requires special controls. | 135 |