Duns Number:811313428
Device Description: ATRAMAT POLYESTER SURGICAL SUTURE WHITE USP 5-0 EP 1, 45 CM DOUBLE NEEDLE E-EA-8 SUPRAGLYD ATRAMAT POLYESTER SURGICAL SUTURE WHITE USP 5-0 EP 1, 45 CM DOUBLE NEEDLE E-EA-8 SUPRAGLYDE SPATULA 8 MM 1/4 CIRCLEPOLIESTER BLANCO USP 5-0, 45 CM DOBLE AGUJA E-EA-8 ESPATULADA SUPRAGLYDE 8 MM 1/4 CIRCULO
Catalog Number
E-EA855/2-45B
Brand Name
ATRAMAT
Version/Model Number
POLIESTER
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
K905285,K905285
Product Code
GAS
Product Code Name
Suture, Nonabsorbable, Synthetic, Polyester
Public Device Record Key
d1170648-7eb6-4a93-aa8d-a9d3b1e6dbd2
Public Version Date
February 05, 2021
Public Version Number
3
DI Record Publish Date
July 16, 2018
Package DI Number
07500142168765
Quantity per Package
12
Contains DI Package
07500142068768
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 |