Duns Number:542984702
Catalog Number
-
Brand Name
NA
Version/Model Number
AG-5332-241523
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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
K172727,K172727,K172727,K172727,K172727,K172727,K172727
Product Code
PKL
Product Code Name
Hemostatic Metal Clip For The Gi Tract
Public Device Record Key
019dd1e9-6166-4654-9e23-70593f06f5cf
Public Version Date
May 02, 2019
Public Version Number
1
DI Record Publish Date
April 24, 2019
Package DI Number
66959664909562
Quantity per Package
10
Contains DI Package
56959664909565
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 2 |