Duns Number:961027315
Device Description: KIT,GYN LAPAROSCOPY
Catalog Number
PBV8LSASF5
Brand Name
CARDINAL HEALTH
Version/Model Number
PBV8LSASF5
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"
Yes
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
OHD
Product Code Name
Gynecological laparoscopic kit
Public Device Record Key
bf61c8b1-7227-4583-9e04-9b3c61faae26
Public Version Date
November 12, 2018
Public Version Number
1
DI Record Publish Date
October 11, 2018
Package DI Number
50888439210000
Quantity per Package
1
Contains DI Package
10888439210002
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 101686 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 139430 |
| 3 | A medical device with high risk that requires premarket approval | 8 |
| U | Unclassified | 40 |