Duns Number:961027315
Device Description: ACTI-GARD Antimicrobial Incise Drape 6" x 7.5"
Catalog Number
D6635
Brand Name
CONVERTORS
Version/Model Number
D6635
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 03, 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
KKX
Product Code Name
Drape, surgical
Public Device Record Key
0f21f8e4-cdab-4917-b8ca-b9ff375fbeec
Public Version Date
May 03, 2022
Public Version Number
7
DI Record Publish Date
June 28, 2016
Package DI Number
50885380071629
Quantity per Package
10
Contains DI Package
10885380071621
Package Discontinue Date
May 03, 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 |