Duns Number:080578874
Device Description: Resorbable Borate Glass Wound Management Device
Catalog Number
-
Brand Name
MIRRAGEN® Advanced Wound Matrix
Version/Model Number
MET-0101
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K161067,K161067
Product Code
FRO
Product Code Name
Dressing, Wound, Drug
Public Device Record Key
b2d30218-764d-46e2-bde5-f526d9a138a3
Public Version Date
July 09, 2020
Public Version Number
4
DI Record Publish Date
February 14, 2020
Package DI Number
00812005030056
Quantity per Package
10
Contains DI Package
00812005030025
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
Device Class | Device Class Description | No of Devices |
---|---|---|
U | Unclassified | 5 |