Duns Number:440211428
Device Description: FRANSEEN fine aspiration needle 18G x 160MM
Catalog Number
-
Brand Name
FRANSEEN
Version/Model Number
FR18160-01
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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"
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
KNW
Product Code Name
Instrument, Biopsy
Public Device Record Key
1d4653f2-fbbe-4b3c-8004-040558b1e056
Public Version Date
October 10, 2019
Public Version Number
1
DI Record Publish Date
October 02, 2019
Package DI Number
18056772677611
Quantity per Package
20
Contains DI Package
08056772677614
Package Discontinue Date
-
Package Status
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 | 24 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 436 |