Duns Number:879187821
Device Description: REDILON Monofilament Polyamide (Nylon), Black, 4-0, MFS-2
Catalog Number
-
Brand Name
RELI
Version/Model Number
N662-SI
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
b519004e-20fe-4ae4-a1bb-ab4a595242a0
Public Version Date
February 05, 2021
Public Version Number
4
DI Record Publish Date
October 24, 2015
Package DI Number
20386120005953
Quantity per Package
30
Contains DI Package
10386120005956
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 7 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 471 |