Duns Number:177939027
Device Description: Posey Single-Patient Use Bed Pad Sensor - 13" x 32"
Catalog Number
-
Brand Name
Posey
Version/Model Number
8283
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
July 10, 2019
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
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
-
Product Code
KMI
Product Code Name
Monitor, Bed Patient
Public Device Record Key
5d155e9b-1b8b-49f7-8706-3055c880cade
Public Version Date
March 19, 2021
Public Version Number
4
DI Record Publish Date
September 24, 2016
Package DI Number
30817357020633
Quantity per Package
6
Contains DI Package
10817357020639
Package Discontinue Date
March 19, 2021
Package Status
Not in Commercial Distribution
Package Type
Box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 49 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 178 |