Duns Number:184805166
Device Description: 7F 40 cm NovaSil Silicone Single Lumen Embolectomy Catheter, eIFU
Catalog Number
e1801-74
Brand Name
LeMaitre Embolectomy Catheter
Version/Model Number
e1801-74
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
K992368
Product Code
DXE
Product Code Name
Catheter, Embolectomy
Public Device Record Key
348912f8-654b-4b16-9bba-a585680240f2
Public Version Date
October 24, 2022
Public Version Number
5
DI Record Publish Date
July 15, 2015
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 22 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 453 |
| 3 | A medical device with high risk that requires premarket approval | 22 |