Duns Number:688432407
Catalog Number
-
Brand Name
Miracu FC BI 21Gx90mm
Version/Model Number
F-FTN2192G
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
K172602,K172602,K172602,K172602
Product Code
NEW
Product Code Name
Suture, Surgical, Absorbable, Polydioxanone
Public Device Record Key
c3f43c5a-b00d-4d51-a7dd-3a41517f1998
Public Version Date
February 05, 2021
Public Version Number
3
DI Record Publish Date
December 24, 2019
Package DI Number
38809407786738
Quantity per Package
300
Contains DI Package
28809407786731
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CARTON BOX
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 2 |