Duns Number:121622872
Device Description: RBN-114S P/N 74092-01M
Catalog Number
RBN-114S
Brand Name
NDL, RBN-114S, STERILE, F/G
Version/Model Number
11GA X 4"
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
K983187,K983187,K983187
Product Code
KNW
Product Code Name
Instrument, Biopsy
Public Device Record Key
6ace3764-1a9e-459c-8851-fd5193ac1596
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
May 08, 2017
Package DI Number
20858690006048
Quantity per Package
12
Contains DI Package
10858690006041
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 | 31 |
2 | A medical device with a moderate to high risk that requires special controls. | 93 |