Duns Number:811313428
Device Description: ATRAMAT SILK SURGICAL SUTURE BLACK USP 4-0 EP 1,5, 45 CM DOUBLE NEEDLE P-PE-13 SUPRA-SHARP ATRAMAT SILK SURGICAL SUTURE BLACK USP 4-0 EP 1,5, 45 CM DOUBLE NEEDLE P-PE-13 SUPRA-SHARP REVERSE CUTTING 13 MM 3/8 CIRCLESEDA NEGRA USP 4-0, 45 CM DOBLE AGUJA P-PE-13 REVERSO CORTANTE SUPRA-SHARP 13 MM 3/8 CIRCULO
Catalog Number
P-PE1334/2
Brand Name
ATRAMAT
Version/Model Number
SEDA
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"
-
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
K905287,K905287
Product Code
GAP
Product Code Name
Suture, Nonabsorbable, Silk
Public Device Record Key
974578b1-7c85-4863-bae1-37d7debdcfcc
Public Version Date
February 05, 2021
Public Version Number
5
DI Record Publish Date
October 17, 2016
Package DI Number
07500142156212
Quantity per Package
12
Contains DI Package
07500142056215
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 |