Duns Number:811313428
Device Description: ATRAMAT POLYPROPYLENE SURGICAL SUTURE BLUE USP 2 EP 5, 3 X 50 CM NEEDLE PE-75 PREMIUM REVE ATRAMAT POLYPROPYLENE SURGICAL SUTURE BLUE USP 2 EP 5, 3 X 50 CM NEEDLE PE-75 PREMIUM REVERSE CUTTING 75 MM 3/8 CIRCLEPOLIPROPILENO AZUL USP 2, 3 X 50 CM AGUJA PE-75 REVERSO CORTANTE PREMIUM 75 MM 3/8 CIRCULO
Catalog Number
PE7569-50X3
Brand Name
ATRAMAT
Version/Model Number
POLIPROPILENO
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
December 31, 2040
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"
Yes
For Single-Use
Yes
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K911189,K911189
Product Code
GAW
Product Code Name
Suture, Nonabsorbable, Synthetic, Polypropylene
Public Device Record Key
cbc7533e-1d23-4f5e-b549-0ba46b7c7832
Public Version Date
February 05, 2021
Public Version Number
3
DI Record Publish Date
July 30, 2018
Package DI Number
07500142180620
Quantity per Package
12
Contains DI Package
07500142080623
Package Discontinue Date
December 31, 2040
Package Status
In Commercial Distribution
Package Type
DOZEN
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 44 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 830 |