Duns Number:196548481
Device Description: System without Needles with Bone Cement
Catalog Number
0605-687-000
Brand Name
AutoPlex, VertaPlex
Version/Model Number
0605687000
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
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
JDZ
Product Code Name
MIXER, CEMENT, FOR CLINICAL USE
Public Device Record Key
87cf83b8-134f-4032-b7ff-2577669f7381
Public Version Date
August 01, 2019
Public Version Number
5
DI Record Publish Date
December 29, 2016
Package DI Number
37613154687160
Quantity per Package
2
Contains DI Package
07613154687169
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
pack
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 2188 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 3183 |
| U | Unclassified | 60 |