Duns Number:711091157
Catalog Number
342002
Brand Name
Kitazato OPU Reduced Needle, Type3-v7
Version/Model Number
342002 Type3-v7
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
aeff906e-c342-479a-80b9-24029d50bb6d
Public Version Date
March 29, 2021
Public Version Number
4
DI Record Publish Date
May 30, 2018
Package DI Number
14580303269326
Quantity per Package
10
Contains DI Package
04580303269329
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 |