Duns Number:879187821
Device Description: REDILON PRO BLK MF 4-0 YFS-2 10"
Catalog Number
N6621-M
Brand Name
RELI®
Version/Model Number
N6621-M
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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"
Yes
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
K172149,K172149,K172149
Product Code
GAR
Product Code Name
Suture, Nonabsorbable, Synthetic, Polyamide
Public Device Record Key
99d406e4-3764-4347-bd31-06ec17cba983
Public Version Date
September 23, 2021
Public Version Number
1
DI Record Publish Date
September 15, 2021
Package DI Number
10386120011742
Quantity per Package
12
Contains DI Package
00386120011745
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Inner Carton
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 |