MAMORAY HD S - MAMORAY CASSETTE / HD S - AGFA

Duns Number:374444883

Device Description: MAMORAY CASSETTE / HD S

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More Product Details

Catalog Number

EDBZJ

Brand Name

MAMORAY HD S

Version/Model Number

MAMORAY HD S 18X24

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

-

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

K790273

Product Code Details

Product Code

IZH

Product Code Name

System, x-ray, mammographic

Device Record Status

Public Device Record Key

80131378-971c-40be-8ea7-ea0c477121e4

Public Version Date

June 14, 2019

Public Version Number

4

DI Record Publish Date

September 01, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"AGFA" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 202