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

Duns Number:811313428

Device Description: ATRAMAT POLYPROPYLENE SURGICAL SUTURE BLUE USP 3-0 EP 2, 75 CM NEEDLE CE-24 REVERSE CUTT ATRAMAT POLYPROPYLENE SURGICAL SUTURE BLUE USP 3-0 EP 2, 75 CM NEEDLE CE-24 REVERSE CUTTING 24 MM 3/8 CIRCLEPOLIPROPILENO AZUL USP 3-0, 75 CM AGUJA CE-24 REVERSO CORTANTE 24 MM 3/8 CIRCULO

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More Product Details

Catalog Number

CE2463-75

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

b0716b6c-ddd6-4ce9-9c1f-0249b1ba91f6

Public Version Date

February 05, 2021

Public Version Number

3

DI Record Publish Date

July 04, 2018

Additional Identifiers

Package DI Number

07500142100383

Quantity per Package

12

Contains DI Package

07500142000386

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