Catalog Number
HNY-88770
Brand Name
Hexa
Version/Model Number
HNY-88770
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
GAP
Product Code Name
SUTURE, NONABSORBABLE, SILK
Public Device Record Key
9ac88871-59f2-4624-89e3-8d8ca0c8e6ba
Public Version Date
February 05, 2021
Public Version Number
3
DI Record Publish Date
December 09, 2020
Package DI Number
00850023750242
Quantity per Package
12
Contains DI Package
00850023750013
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
PACK
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 32 |
2 | A medical device with a moderate to high risk that requires special controls. | 15 |