Duns Number:961027315
Device Description: LAPAROSCOPIC LITHOTOMY PACK
Catalog Number
SLC30LIQED
Brand Name
CARDINAL HEALTH
Version/Model Number
SLC30LIQED
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
October 19, 2017
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
1eaade7e-885d-4b8b-87ed-0942197b79c8
Public Version Date
October 22, 2018
Public Version Number
4
DI Record Publish Date
October 19, 2015
Package DI Number
50887488021407
Quantity per Package
2
Contains DI Package
00887488021402
Package Discontinue Date
October 19, 2017
Package Status
Not 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 |