MONOSWIFT - C.P. MEDICAL CORPORATION

Duns Number:807404611

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More Product Details

Catalog Number

L492

Brand Name

MONOSWIFT

Version/Model Number

L492

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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

K072229,K072229

Product Code Details

Product Code

GAM

Product Code Name

Suture, Absorbable, Synthetic, Polyglycolic Acid

Device Record Status

Public Device Record Key

b980036b-aac5-4511-99e1-139da8535538

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

June 13, 2016

Additional Identifiers

Package DI Number

20790986001408

Quantity per Package

12

Contains DI Package

10790986001401

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"C.P. MEDICAL CORPORATION" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 461