Duns Number:076916246
Device Description: Base Assembly Only, Adjustable, Painted (For 9805P Hydraulic Lift)
Catalog Number
9884P
Brand Name
Base Assembly Only, Adjustable, Painted (For 9805P Hydraulic Lift)
Version/Model Number
9884P
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)
Yes
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
538fbce9-f4e8-4f8b-9499-0c26a230ab50
Public Version Date
June 18, 2019
Public Version Number
1
DI Record Publish Date
June 10, 2019
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 | 136 |
2 | A medical device with a moderate to high risk that requires special controls. | 273 |