Duns Number:945385862
Device Description: OASIS Wound Matrix
Catalog Number
8213-2000-37
Brand Name
OASIS
Version/Model Number
G46627
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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
K061711,K061711
Product Code
KGN
Product Code Name
Dressing, wound, collagen
Public Device Record Key
f2c5688a-ff02-4408-b2cd-dd2ce6d070a1
Public Version Date
April 25, 2019
Public Version Number
1
DI Record Publish Date
April 17, 2019
Package DI Number
10827002466279
Quantity per Package
10
Contains DI Package
00827002466272
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 2 |
2 | A medical device with a moderate to high risk that requires special controls. | 116 |
U | Unclassified | 36 |