Duns Number:021063219
Device Description: Emergency response system for field deployable ED overflow needs
Catalog Number
A-WSS-001-ZA
Brand Name
Emergency Response System
Version/Model Number
A-WSS-001-ZA
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
April 29, 2020
Issuing Agency
In GS1
MRI safety Status
MR Unsafe
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
DRG
Product Code Name
TRANSMITTERS AND RECEIVERS, PHYSIOLOGICAL SIGNAL, RADIOFREQUENCY
Public Device Record Key
9d01b09b-9add-41f9-aee4-769ea250d1b0
Public Version Date
November 10, 2021
Public Version Number
4
DI Record Publish Date
April 20, 2020
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 | 1 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 393 |