Duns Number:256880576
Device Description: SAFESEAL QUATTRO 10 X 14 IN
Catalog Number
88035-4
Brand Name
MEDICOM SAFESEAL QUATTRO
Version/Model Number
88035-4
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)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
KCT
Product Code Name
Sterilization wrap containers, trays, cassettes & other accessories
Public Device Record Key
94e3e802-813d-4f37-a5d8-5eb294be8861
Public Version Date
November 08, 2019
Public Version Number
4
DI Record Publish Date
September 15, 2016
Package DI Number
20686864045827
Quantity per Package
5
Contains DI Package
10686864045820
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
OUTER CASE
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 84 |
2 | A medical device with a moderate to high risk that requires special controls. | 27 |
U | Unclassified | 2 |