Duns Number:342243334
Device Description: K-Wire w. double end lanzet point 1.1mm/229mm, 6 pcs./unit
Catalog Number
KM71-212
Brand Name
K-Wire w. double end lanzet point 1.1mm/229mm, 6 pcs./unit
Version/Model Number
KM71-212
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
MRI safety Status
MR Safe
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
HTY
Product Code Name
PIN, FIXATION, SMOOTH
Public Device Record Key
5c501899-af7a-48f8-90c5-243a9c815b94
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
April 28, 2016
Package DI Number
EMAHKM712121
Quantity per Package
1
Contains DI Package
EMAHKM712120
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 | 19 |
2 | A medical device with a moderate to high risk that requires special controls. | 1976 |