Duns Number:012430880
Device Description: HS C17 5-0 BK MN NYL 10"/25CM
Catalog Number
900-7459
Brand Name
Henry Schein
Version/Model Number
900-7459
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
GAR
Product Code Name
SUTURE, NONABSORBABLE, SYNTHETIC, POLYAMIDE
Public Device Record Key
6f59e8d6-4f0b-4c29-9e8d-328bbf9bdc8a
Public Version Date
February 05, 2021
Public Version Number
4
DI Record Publish Date
September 25, 2015
Package DI Number
20304040000063
Quantity per Package
12
Contains DI Package
00304040000069
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 3829 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 2579 |
| 3 | A medical device with high risk that requires premarket approval | 1 |
| U | Unclassified | 34 |