Duns Number:533108028
Catalog Number
12003-000-0013
Brand Name
AP403-01 - MICROBORE WITH NON-VENTED SPIKE
Version/Model Number
12003-000-0013
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"
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
K141389,K141389
Product Code
FPA
Product Code Name
Set, Administration, Intravascular
Public Device Record Key
7bd75f1b-f499-4d63-99e7-0cb18e7fc855
Public Version Date
June 20, 2019
Public Version Number
1
DI Record Publish Date
June 12, 2019
Package DI Number
27290109159199
Quantity per Package
30
Contains DI Package
17290109159192
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Cardboard box
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 65 |