Duns Number:811313428
Device Description: ATRAMAT POLYPROPYLENE SURGICAL SUTURE BLUE USP 7-0 EP 0.5, 60 CM DOUBLE NEEDLE CVSVE-9.3 C ATRAMAT POLYPROPYLENE SURGICAL SUTURE BLUE USP 7-0 EP 0.5, 60 CM DOUBLE NEEDLE CVSVE-9.3 CARDIOVASCULAR SUPRAGLYDE TAPER POINT (Non Reflective Dark Needle) 9.3 MM 3/8 CIRCLEPOLIPROPILENO AZUL USP 7-0, 60 CM DOBLE AGUJA CVSVE-9.3 CARDIOVASCULAR AHUSADA SUPRAGLYDE (ANTIRREFLEJANTE NEGRA) 9.3 MM 3/8 CIRCULO
Catalog Number
CVSVE9.367/2-60
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
86e17584-7211-44fe-ae85-f05005778d52
Public Version Date
February 05, 2021
Public Version Number
3
DI Record Publish Date
July 30, 2018
Package DI Number
07500142180156
Quantity per Package
12
Contains DI Package
07500142080159
Package Discontinue Date
July 31, 2018
Package Status
Not 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 |