Duns Number:002348191
Device Description: Expro Elite Snare V2 5mm
Catalog Number
8400
Brand Name
EXPRO ELITE
Version/Model Number
IPN913614
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"
-
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
MMX
Product Code Name
Device, percutaneous retrieval
Public Device Record Key
e41f5b72-c2a5-4880-a9a1-107c78db06d8
Public Version Date
July 08, 2021
Public Version Number
3
DI Record Publish Date
November 08, 2018
Package DI Number
30841156101514
Quantity per Package
1
Contains DI Package
10841156101510
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 | 3195 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 13747 |
| 3 | A medical device with high risk that requires premarket approval | 3 |
| U | Unclassified | 26 |