Duns Number:021717889
Device Description: Introducer Needle
Catalog Number
-
Brand Name
AccuStick™ Needle
Version/Model Number
H7493937021200
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
GCB
Product Code Name
NEEDLE, CATHETER
Public Device Record Key
a8990119-08ab-4094-8c50-74de5d537bfb
Public Version Date
June 07, 2019
Public Version Number
3
DI Record Publish Date
August 17, 2016
Package DI Number
08714729862918
Quantity per Package
10
Contains DI Package
08714729862932
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 | 536 |
2 | A medical device with a moderate to high risk that requires special controls. | 8659 |
3 | A medical device with high risk that requires premarket approval | 1821 |
U | Unclassified | 35 |