Duns Number:073436164
Device Description: Sterilization Pouch, SS, 5 1/4" x 10"
Catalog Number
-
Brand Name
IMCO
Version/Model Number
1525-IMC
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)
-
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
75786636-74ee-46c8-9eb1-2b36c08c63e5
Public Version Date
November 08, 2019
Public Version Number
3
DI Record Publish Date
June 20, 2016
Package DI Number
20815842023148
Quantity per Package
10
Contains DI Package
10815842023141
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 1 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 42 |