Duns Number:175254820
Catalog Number
-
Brand Name
Custom Healthcare Systems Inc.
Version/Model Number
R1668
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
FQM
Product Code Name
Bandage, Elastic
Public Device Record Key
960fe7c8-f5d5-41f7-b42e-10cc0a28c2f2
Public Version Date
August 27, 2018
Public Version Number
1
DI Record Publish Date
July 26, 2018
Package DI Number
20811870030905
Quantity per Package
36
Contains DI Package
00811870030901
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
N/A
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 210 |
2 | A medical device with a moderate to high risk that requires special controls. | 304 |