Duns Number:002348191
Device Description: STL MFCOMPAK 5 2(K-60)/6(B-60) 18"X8
Catalog Number
29-9008M8
Brand Name
DEKNATEL
Version/Model Number
IPN004809
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Unsafe
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
3c67faa8-145b-4d00-afd8-ff87a8056c31
Public Version Date
February 05, 2021
Public Version Number
7
DI Record Publish Date
October 16, 2015
Package DI Number
24026704590135
Quantity per Package
6
Contains DI Package
04026704590131
Package Discontinue Date
August 31, 2018
Package Status
Not 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 |