Duns Number:015272206
Device Description: ArthVance® cupped grasping forceps, 3.3mm cupped jaw, atraumatic, straight shaft, pro hand ArthVance® cupped grasping forceps, 3.3mm cupped jaw, atraumatic, straight shaft, pro handle
Catalog Number
26-203
Brand Name
Ambler Surgical
Version/Model Number
ArthVance® cupped grasping forceps
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
-
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
LRY
Product Code Name
PUNCH, SURGICAL
Public Device Record Key
a7bd1112-f3d4-441c-b19d-0d76aa4e3931
Public Version Date
October 19, 2021
Public Version Number
2
DI Record Publish Date
January 07, 2021
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 | 14984 |
2 | A medical device with a moderate to high risk that requires special controls. | 3118 |