Duns Number:812762226
Device Description: 2xDDSL-9.4-230 black USP 7-0 Polypropylene blue 75 cm. sterile. 36pcs. Per Box VA10.1
Catalog Number
D9B-773K
Brand Name
FUMEDICA
Version/Model Number
D9B-773K
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
K131224,K131224
Product Code
GAW
Product Code Name
Suture, nonabsorbable, synthetic, polypropylene
Public Device Record Key
db016e74-5452-4348-96f0-ea266a033ae1
Public Version Date
August 29, 2022
Public Version Number
2
DI Record Publish Date
October 22, 2021
Package DI Number
10848782041944
Quantity per Package
36
Contains DI Package
00848782041947
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 | 300 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 2030 |
| U | Unclassified | 19 |