Duns Number:040729840
Device Description: WIRE CUTTER WITHOUT SPRINGS SINGLE ACTION UP-ANGLE TUNGSTEN CARBIDE BLADE
Catalog Number
1103-112
Brand Name
WIRE CUTTER
Version/Model Number
1103-112
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
-
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
HXZ
Product Code Name
Cutter, Wire
Public Device Record Key
0d35b7bd-ee26-4e38-82f4-aa07839bdb7b
Public Version Date
June 03, 2019
Public Version Number
2
DI Record Publish Date
May 03, 2019
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 | 10108 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 3414 |