Duns Number:012430880
Device Description: HS C8 2-0 BK MN NYL 18"/45CM
Catalog Number
900-7476
Brand Name
Henry Schein
Version/Model Number
900-7476
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
022e2385-42c3-464f-bed3-91a104354584
Public Version Date
February 05, 2021
Public Version Number
4
DI Record Publish Date
September 25, 2015
Package DI Number
20304040000148
Quantity per Package
12
Contains DI Package
00304040000144
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 |