Percutaneous Micro Introducer Kit - Percutaneous Micro Introducer Kit 5F - ARGON MEDICAL DEVICES, INC.

Duns Number:140727624

Device Description: Percutaneous Micro Introducer Kit 5F

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More Product Details

Catalog Number

497819

Brand Name

Percutaneous Micro Introducer Kit

Version/Model Number

497819

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)

Yes

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

OFL

Product Code Name

Percutaneous Sheath Introducer Kit

Device Record Status

Public Device Record Key

7867fa72-5717-4f5a-b12f-0de576e3e63f

Public Version Date

June 07, 2019

Public Version Number

3

DI Record Publish Date

September 16, 2016

Additional Identifiers

Package DI Number

10886333215086

Quantity per Package

10

Contains DI Package

00886333215089

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box

"ARGON MEDICAL DEVICES, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 347
2 A medical device with a moderate to high risk that requires special controls. 1205