Duns Number:811313428
Device Description: ATRAMAT SILK SURGICAL SUTURE BLACK USP 3-0 EP 2, 45 CM NEEDLE PE-24 PREMIUM REVERSE CUTTIN ATRAMAT SILK SURGICAL SUTURE BLACK USP 3-0 EP 2, 45 CM NEEDLE PE-24 PREMIUM REVERSE CUTTING 24 MM 3/8 CIRCLESEDA NEGRA USP 3-0, 45 CM AGUJA PE-24 REVERSO CORTANTE PREMIUM 24 MM 3/8 CIRCULO
Catalog Number
PE2433-45
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"
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
K905287,K905287
Product Code
GAP
Product Code Name
Suture, Nonabsorbable, Silk
Public Device Record Key
223023c1-18db-4987-b7a5-6384ff23ba00
Public Version Date
February 05, 2021
Public Version Number
2
DI Record Publish Date
July 16, 2018
Package DI Number
07500142129896
Quantity per Package
12
Contains DI Package
07500142029899
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 |