Duns Number:053469565
Device Description: Male - Male Luer Slip Adapter. Sterile & Non-Pyrogenic, Individually Blister Packed, Box o Male - Male Luer Slip Adapter. Sterile & Non-Pyrogenic, Individually Blister Packed, Box of 50
Catalog Number
57-02-50
Brand Name
Male-Male Luer Slip Adapter
Version/Model Number
57-02-50
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
FPA
Product Code Name
Set, Administration, Intravascular
Public Device Record Key
c8956c13-f32d-4e5b-be3b-3462c63b31e0
Public Version Date
September 29, 2022
Public Version Number
1
DI Record Publish Date
September 21, 2022
Package DI Number
B2125702502
Quantity per Package
50
Contains DI Package
B2125702501
Package Discontinue Date
-
Package Status
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 | 6 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 15 |