Duns Number:711091157
Device Description: 3Fr 400mm Catheter, Guide with obturator
Catalog Number
223340
Brand Name
Kitazato ET Catheter
Version/Model Number
223340 Type2-v5
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
MQF
Product Code Name
CATHETER, ASSISTED REPRODUCTION
Public Device Record Key
eeaf7f0d-a050-41d2-9d84-66cacd36d324
Public Version Date
March 29, 2021
Public Version Number
2
DI Record Publish Date
November 26, 2020
Package DI Number
14580303266141
Quantity per Package
10
Contains DI Package
04580303266144
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 |