Duns Number:811313428
Device Description: ATRAMAT NYLON SURGICAL SUTURE BLACK USP 2-0 EP 3, 75 CM NEEDLE P-PE-24 SUPRA-SHARP REVERSE ATRAMAT NYLON SURGICAL SUTURE BLACK USP 2-0 EP 3, 75 CM NEEDLE P-PE-24 SUPRA-SHARP REVERSE CUTTING 24 MM 3/8 CIRCLENYLON NEGRO USP 2-0, 75 CM AGUJA P-PE-24 REVERSO CORTANTE SUPRA-SHARP 24 MM 3/8 CIRCULO
Catalog Number
P-PE2442-75N
Brand Name
ATRAMAT
Version/Model Number
NYLON
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
K905286,K905286
Product Code
GAR
Product Code Name
Suture, Nonabsorbable, Synthetic, Polyamide
Public Device Record Key
b9100980-27c1-462a-bd1b-5f4181a68e04
Public Version Date
February 05, 2021
Public Version Number
3
DI Record Publish Date
July 16, 2018
Package DI Number
07500142179600
Quantity per Package
12
Contains DI Package
07500142079603
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 |