Duns Number:080935429
Device Description: AMD Antimicrobial Drain Sponges, 6 Ply, 0.2% Polyhexamethylene Biguanide HCI (PHMB)
Catalog Number
7088
Brand Name
Excilon
Version/Model Number
7088
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
K011941,K011941,K011941,K011941
Product Code
EFQ
Product Code Name
GAUZE/SPONGE, INTERNAL
Public Device Record Key
2ae4d405-bd7d-47da-b8a6-090913cf259d
Public Version Date
June 19, 2020
Public Version Number
3
DI Record Publish Date
June 28, 2018
Package DI Number
20884521020181
Quantity per Package
600
Contains DI Package
00884521020187
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 | 672 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1692 |
| U | Unclassified | 17 |