Duns Number:131107757
Catalog Number
40-1520
Brand Name
OptiMatrix™ Extracellular Matrix
Version/Model Number
30053-01
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 30, 2019
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
-
Product Code
NPL
Product Code Name
Barrier, Animal Source, Intraoral
Public Device Record Key
eff462ca-64cf-49f7-9077-39b1ba2b5993
Public Version Date
October 01, 2019
Public Version Number
4
DI Record Publish Date
September 16, 2015
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 9 |
2 | A medical device with a moderate to high risk that requires special controls. | 132 |
U | Unclassified | 5 |