Duns Number:447228586
Device Description: 10 CS -SEMIAUTOMATICNEEDLE18G X 160MM WITHOUT REMOVABLELUER WITH INTRODUCER
Catalog Number
PD0PP1816
Brand Name
SemiCut
Version/Model Number
PD0PP1816
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 13, 2021
Issuing Agency
In GS1
MRI safety Status
MR Unsafe
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"
-
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
K160316,K160316
Product Code
FCG
Product Code Name
Biopsy Needle
Public Device Record Key
26cbbee0-6ff9-4ba1-8f32-74b1f457a225
Public Version Date
May 27, 2021
Public Version Number
7
DI Record Publish Date
January 04, 2017
Package DI Number
08052440100521
Quantity per Package
10
Contains DI Package
08058341214367
Package Discontinue Date
May 13, 2021
Package Status
Not in Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 228 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 138 |