Duns Number:002348191
Device Description: STL MF 1 C-2 1N 18"X5
Catalog Number
X-6730M5
Brand Name
DEKNATEL
Version/Model Number
IPN027102
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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
-
Product Code
GAQ
Product Code Name
Suture, nonabsorbable, steel, monofilament and multifilament, sterile
Public Device Record Key
4f0f4703-1aad-43f3-9f6d-86fccceb1b36
Public Version Date
February 05, 2021
Public Version Number
4
DI Record Publish Date
July 26, 2018
Package DI Number
14026704427816
Quantity per Package
12
Contains DI Package
34026704427810
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 3195 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 13747 |
| 3 | A medical device with high risk that requires premarket approval | 3 |
| U | Unclassified | 26 |