Mammomat Fusion

Ffdm

Registry build 21.09.26
1manufacturer
1catalogue number

Who Else Makes It

Registered in Jiangsu.

Chinese manufacturers registered for FDA product code MUE
Manufacturer City Province Registered as Device types
Fujifilm Imaging System (Suzhou) Co., Ltd. Suzhou Jiangsu Manufacturer 3

Record

Regulatory record for Mammomat Fusion
Listed by Siemens Healthcare Limited, Canada
FDA product code MUE
Device type Full Field Digital, System, X-Ray, Mammographic
Device class Class 2
Regulation 21 CFR 892.1715
Establishment Contract manufacturer, Manufacturer, Exporter
Record published 2016-09-24
Record revised 2021-11-18 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries serial number

Catalogue Numbers

Catalogue numbers for Mammomat Fusion
Catalogue number Size Status
10762444 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Selenia® Dimensions® Hologic, Inc. 47
Selenia Ffdm Hologic, Inc. 29
Full Field Digital, System, X-Ray, Mammographic GE Medical Systems, LLC 10
Senographe Pristina GE Medical Systems, LLC 10
Directview CR Mammography Cassette with EHR-M Screen Carestream Health, Inc. 10
Giotto Class IMS Giotto SPA 6
Directview CR Mammography Cassette with EHR-M3 Screen Carestream Health, Inc. 5
Giotto Image 3DL I.M.S. Internazionale Medico Scientifica SRL 5
CR-IR 392 Fujifilm Corporation 3
Giotto Image IMS Giotto SPA 3
CR HD5.0 AEC Cassette Agfa Healthcare Inc. 3
Directview CR Mammography Cassette with HR Screen Carestream Health, Inc. 3

Showing 12 of 103. All products under Full Field Digital, System, X-Ray, Mammographic

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P080018 2010-11-03 KODAK DIRECTVIEW COMPUTED RADIOGRAPHY (CR) MAMMOGRAPHY Carestream Health, Inc.
P050014 2009-01-09 FUJI COMPUTED RADIOGRAPHY MAMMOGRAPHY SUITE Fujifilm Medical System U.S.A., Inc.
P990066 2007-08-01 GE SENOGRAPHE ESSENTIAL FULL FIELD MAMMOGRAPHY SYSYTEM (SENO ESSENTIAL GE Healthcare GmbH
P030010 2004-08-20 SIEMENS MAMMOMAT NOVATIONDR FULL FIELD DIGITAL MAMMOGRAPHY SYSTEM Siemens Medical Solution
P010017 2004-05-12 SENOSCAN FULL FIELD DIGITAL MAMMOGRAPHY SYSTEM Hologic, Inc.
P010025 2003-09-24 SELENIA FULL FIELD DIGITAL MAMMOGRAPHY SYSTEM Hologic, Inc.

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer