Merit Advance® - Merit Medical Systems, Inc.

Duns Number:184763290

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More Product Details

Catalog Number

-

Brand Name

Merit Advance®

Version/Model Number

00884450249154

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

-

Product Code Details

Product Code

DRC

Product Code Name

Trocar

Device Record Status

Public Device Record Key

4c49726e-1de7-47e5-9345-18e6ec9eea3d

Public Version Date

April 07, 2021

Public Version Number

4

DI Record Publish Date

September 28, 2016

Additional Identifiers

Package DI Number

10884450249151

Quantity per Package

25

Contains DI Package

00884450249154

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"MERIT MEDICAL SYSTEMS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 573
2 A medical device with a moderate to high risk that requires special controls. 8779