ATRAMAT - ATRAMAT PGLA90 SURGICAL SUTURE VIOLET USP 0 EP - Internacional Farmacéutica, S.A. de C.V.

Duns Number:811313428

Device Description: ATRAMAT PGLA90 SURGICAL SUTURE VIOLET USP 0 EP 3,5, 70 CM NEEDLE P-26 PREMIUM REVERSE CUTT ATRAMAT PGLA90 SURGICAL SUTURE VIOLET USP 0 EP 3,5, 70 CM NEEDLE P-26 PREMIUM REVERSE CUTTING 26 MM 1/2 CIRCLEPGLA90 VIOLETA USP 0, 70 CM AGUJA P-26 REVERSO CORTANTE PREMIUM 26 MM 1/2 CIRCULO

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More Product Details

Catalog Number

P26301

Brand Name

ATRAMAT

Version/Model Number

PGLA 90

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"

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

K072863,K072863

Product Code Details

Product Code

GAM

Product Code Name

Suture, Absorbable, Synthetic, Polyglycolic Acid

Device Record Status

Public Device Record Key

9d9f34d6-e51d-4e57-a962-29c2b2d8f840

Public Version Date

August 30, 2018

Public Version Number

1

DI Record Publish Date

July 30, 2018

Additional Identifiers

Package DI Number

07500142180576

Quantity per Package

12

Contains DI Package

07500142080579

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