ATRAMAT - ATRAMAT POLYPROPYLENE SURGICAL SUTURE BLUE USP 0 - Internacional Farmacéutica, S.A. de C.V.

Duns Number:811313428

Device Description: ATRAMAT POLYPROPYLENE SURGICAL SUTURE BLUE USP 0 EP 3,5, 75 CM NEEDLE G-37 HEAVY TAPER POI ATRAMAT POLYPROPYLENE SURGICAL SUTURE BLUE USP 0 EP 3,5, 75 CM NEEDLE G-37 HEAVY TAPER POINT 37 MM 1/2 CIRCLEPOLIPROPILENO AZUL USP 0, 75 CM AGUJA G-37 AHUSADA GRUESA 37 MM 1/2 CIRCULO

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More Product Details

Catalog Number

G3761-75

Brand Name

ATRAMAT

Version/Model Number

POLIPROPILENO

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

December 31, 2040

Issuing Agency

In GS1

Product Characteristics

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

K911189,K911189

Product Code Details

Product Code

GAW

Product Code Name

Suture, Nonabsorbable, Synthetic, Polypropylene

Device Record Status

Public Device Record Key

15c8e14b-0100-4151-b1ec-e8dfd5e94ee4

Public Version Date

February 05, 2021

Public Version Number

6

DI Record Publish Date

September 30, 2016

Additional Identifiers

Package DI Number

07500142100390

Quantity per Package

12

Contains DI Package

07500142000393

Package Discontinue Date

December 31, 2040

Package Status

In Commercial Distribution

Package Type

DOZEN

"INTERNACIONAL FARMACÉUTICA, S.A. DE C.V." Characteristics
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