Duns Number:811313428
Device Description: ATRAMAT PGA SURGICAL SUTURE UNDYED USP 4-0 EP 1,5, 45 CM NEEDLE P-PE-13 SUPRA-SHARP REVERS ATRAMAT PGA SURGICAL SUTURE UNDYED USP 4-0 EP 1,5, 45 CM NEEDLE P-PE-13 SUPRA-SHARP REVERSE CUTTING 13 MM 3/8 CIRCLEPGA INCOLORO USP 4-0, 45 CM AGUJA P-PE-13 REVERSO CORTANTE SUPRA-SHARP 13 MM 3/8 CIRCULO
Catalog Number
P-PE1394-45B
Brand Name
ATRAMAT
Version/Model Number
PGA
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
K040282,K040282
Product Code
GAM
Product Code Name
Suture, Absorbable, Synthetic, Polyglycolic Acid
Public Device Record Key
efb622d6-633f-4a6e-81e6-8cb62eaaca74
Public Version Date
July 06, 2018
Public Version Number
4
DI Record Publish Date
October 18, 2016
Package DI Number
07500142157493
Quantity per Package
12
Contains DI Package
07500142057496
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 |