Mammotome - Probe Guide - DEVICOR MEDICAL PRODUCTS, INC.

Duns Number:961832156

Device Description: Probe Guide

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More Product Details

Catalog Number

-

Brand Name

Mammotome

Version/Model Number

G08U

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

K943863,K943863

Product Code Details

Product Code

IYN

Product Code Name

System, Imaging, Pulsed Doppler, Ultrasonic

Device Record Status

Public Device Record Key

830ed922-3d03-4f6e-b487-9508427d0ac2

Public Version Date

June 17, 2022

Public Version Number

2

DI Record Publish Date

February 04, 2022

Additional Identifiers

Package DI Number

10841911101199

Quantity per Package

25

Contains DI Package

00841911101192

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"DEVICOR MEDICAL PRODUCTS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 17
2 A medical device with a moderate to high risk that requires special controls. 186