Duns Number:943156836
Device Description: Posi-Stick® Guidewire
Catalog Number
PS2-18
Brand Name
Posi-Stick® Guidewire
Version/Model Number
SGW-068-00
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
K021990,K021990,K021990
Product Code
DQX
Product Code Name
Wire, Guide, Catheter
Public Device Record Key
d9c79adf-f397-4990-9a8b-91610bd15ff4
Public Version Date
December 22, 2021
Public Version Number
2
DI Record Publish Date
January 18, 2019
Package DI Number
20841268108404
Quantity per Package
50
Contains DI Package
10841268108407
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Shipper Box
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 29 |
2 | A medical device with a moderate to high risk that requires special controls. | 696 |