Duns Number:187502109
Device Description: PostFree Patient Safety Kit, Medium
Catalog Number
3105-000-701
Brand Name
Pivot Guardian
Version/Model Number
3105000701
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
LRO
Product Code Name
General surgery tray
Public Device Record Key
ef119b0c-2352-4c7e-9164-ffe7884c00fb
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
September 12, 2017
Package DI Number
37613327376396
Quantity per Package
3
Contains DI Package
07613327376395
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 |