Duns Number:961027315
Device Description: SAFETY BM BIOPSY 11GX4 J TYPE
Catalog Number
31-BM1SF
Brand Name
CARDINAL HEALTH
Version/Model Number
31-BM1SF
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
GAA
Product Code Name
NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE
Public Device Record Key
5d15fe0a-8aaf-4d2e-bc33-dbae1c0c7542
Public Version Date
June 17, 2022
Public Version Number
5
DI Record Publish Date
August 02, 2016
Package DI Number
50885425210242
Quantity per Package
10
Contains DI Package
10885425210244
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 |