Duns Number:691486468
Device Description: Contains: NDL00W-7 (Quantity: 4; Primary DI Number: 04946585249228), NDM00X-7 (Quantity: 4 Contains: NDL00W-7 (Quantity: 4; Primary DI Number: 04946585249228), NDM00X-7 (Quantity: 4; Primary DI Number: 04946585228070), and NDH01Y (Quantity: 2; Primary DI Number: 04946585295584)
Catalog Number
N-SET002
Brand Name
CROWNJUN Nylon Suture
Version/Model Number
N-SET002
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
K192420
Product Code
GAR
Product Code Name
Suture, Nonabsorbable, Synthetic, Polyamide
Public Device Record Key
f68b46a7-dc82-484c-845d-e994ff0f5b47
Public Version Date
March 23, 2021
Public Version Number
1
DI Record Publish Date
March 15, 2021
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. | 12 |