Duns Number:354818510
Device Description: General-purpose patient lifting system sling/harness
Catalog Number
-
Brand Name
Solo MultiStrap™
Version/Model Number
3695916
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
eb52d207-7817-4805-9236-2c87e96906ea
Public Version Date
April 07, 2021
Public Version Number
2
DI Record Publish Date
March 19, 2021
Package DI Number
10887761984216
Quantity per Package
20
Contains DI Package
00887761984219
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 | 267 |