Duns Number:867673159
Device Description: Bath SafetyGrab Bars Product Description: AqS GRAB BAR 24" - KNURL, 12EA/CV
Catalog Number
-
Brand Name
Drive
Version/Model Number
785-106K
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 21, 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
-
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
IKX
Product Code Name
AID, TRANSFER
Public Device Record Key
c75d2da1-9a98-4424-aac6-164eb317d3fc
Public Version Date
June 05, 2020
Public Version Number
3
DI Record Publish Date
June 21, 2019
Package DI Number
50754021216685
Quantity per Package
12
Contains DI Package
00754021216680
Package Discontinue Date
June 21, 2019
Package Status
Not 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 | 3783 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 832 |