Duns Number:961027315
Device Description: Polyethylene Reinforced Towel with Fenestration
Catalog Number
3523CE
Brand Name
CONVERTORS
Version/Model Number
3523CE
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 05, 2022
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
PUI
Product Code Name
Drape, Surgical, Exempt
Public Device Record Key
d4700d43-9e67-4196-aa98-cc0c8a2beda7
Public Version Date
June 06, 2022
Public Version Number
5
DI Record Publish Date
July 14, 2016
Package DI Number
50630140035775
Quantity per Package
50
Contains DI Package
00630140035770
Package Discontinue Date
June 05, 2022
Package Status
Not 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 | 101686 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 139430 |
| 3 | A medical device with high risk that requires premarket approval | 8 |
| U | Unclassified | 40 |