Duns Number:511268005
Device Description: SAFIL QUI + UNDY 4/0(1,5)45CM DS19F(M)
Catalog Number
C1046838
Brand Name
Safil Quick
Version/Model Number
C1046838
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
January 15, 2021
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
GAM
Product Code Name
SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID
Public Device Record Key
84bfe7d1-9fbe-4ae0-821f-9ebff080e51d
Public Version Date
February 05, 2021
Public Version Number
8
DI Record Publish Date
August 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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 13 |