Duns Number:711091157
Catalog Number
351304
Brand Name
Kitazato OPU Needle Type2-v6
Version/Model Number
351304 Type2-v6
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
MQE
Product Code Name
NEEDLE, ASSISTED REPRODUCTION
Public Device Record Key
920c1405-e032-48a8-bc9d-a63a8b289a17
Public Version Date
March 29, 2021
Public Version Number
5
DI Record Publish Date
November 09, 2016
Package DI Number
14580303269142
Quantity per Package
10
Contains DI Package
04580303269145
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 177 |