Duns Number:631805488
Catalog Number
-
Brand Name
Follicle Aspiration Set Reduced Single Lumen
Version/Model Number
17177
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
K172050,K172050
Product Code
MQE
Product Code Name
Needle, Assisted Reproduction
Public Device Record Key
6df675e8-8c32-4772-aa87-99ead6ab9918
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
January 05, 2018
Package DI Number
17350025915453
Quantity per Package
10
Contains DI Package
07350025915456
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 | 1 |
2 | A medical device with a moderate to high risk that requires special controls. | 157 |