Duns Number:867673159
Device Description: Patient RoomSlings Product Description: Sling Full Body Med Mesh 1/bx
Catalog Number
-
Brand Name
Drive
Version/Model Number
13223M
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)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FSA
Product Code Name
LIFT, PATIENT, NON-AC-POWERED
Public Device Record Key
1f103833-58a9-4a89-9770-e3e6cf4b495b
Public Version Date
June 26, 2019
Public Version Number
3
DI Record Publish Date
July 10, 2017
Package DI Number
00822383303673
Quantity per Package
12
Contains DI Package
00822383103679
Package Discontinue Date
-
Package Status
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 |