Duns Number:811313428
Device Description: ATRAMAT PGLA90 SURGICAL SUTURE UNDYED USP 6-0 EP 0.7, 45 CM NEEDLE P-PE-11 SUPRA-SHARP REV ATRAMAT PGLA90 SURGICAL SUTURE UNDYED USP 6-0 EP 0.7, 45 CM NEEDLE P-PE-11 SUPRA-SHARP REVERSE CUTTING 11 MM 3/8 CIRCLEPGLA90 INCOLORO USP 6-0, 45 CM AGUJA P-PE-11 REVERSO CORTANTE SUPRA-SHARP 11 MM 3/8 CIRCULO
Catalog Number
P-PE11306-45B
Brand Name
ATRAMAT
Version/Model Number
PGLA90
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
K072859,K072859
Product Code
GAM
Product Code Name
Suture, Absorbable, Synthetic, Polyglycolic Acid
Public Device Record Key
f39c1714-f911-424c-9e33-5249a6f70ea5
Public Version Date
February 05, 2021
Public Version Number
7
DI Record Publish Date
October 17, 2016
Package DI Number
07500142157325
Quantity per Package
12
Contains DI Package
07500142057328
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 |