Duns Number:121622872
Device Description: RBN-116, F/G, STERILE P/N 74049-02M
Catalog Number
RBN-116
Brand Name
RBN-116, F/G, STERILE
Version/Model Number
11 Gauge X 6"
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
d269566d-d22a-45ba-9fc4-db3812fe4a11
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
February 27, 2017
Package DI Number
10858690006386
Quantity per Package
10
Contains DI Package
00858690006389
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
BOX
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 |