Duns Number:215591523
Catalog Number
-
Brand Name
Wallace
Version/Model Number
AIC18
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
December 12, 2019
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"
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
MFD
Product Code Name
CANNULA, INTRAUTERINE INSEMINATION
Public Device Record Key
1ae137c7-2ca3-4bc8-ba29-ba57ffaf0859
Public Version Date
December 18, 2019
Public Version Number
3
DI Record Publish Date
October 05, 2016
Package DI Number
35019315015704
Quantity per Package
10
Contains DI Package
15019315015700
Package Discontinue Date
December 12, 2019
Package Status
Not in Commercial Distribution
Package Type
Box
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 332 |
2 | A medical device with a moderate to high risk that requires special controls. | 431 |